Canonical Allele Identifier: CA631537152
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1199035222
gnomAD v2: 19-4090714-G-C
gnomAD v4: 19-4090716-G-C
MyVariant Identifiers: chr19:g.4090714G>C (hg19) chr19:g.4090716G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090716G>C , CM000681.2:g.4090716G>C GRCh38
NC_000019.9:g.4090714G>C , CM000681.1:g.4090714G>C GRCh37
NC_000019.8:g.4041714G>C NCBI36
NG_007996.1:g.38413C>G , LRG_750:g.38413C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-8C>G
ENST00000688002.1:n.3244-8C>G
ENST00000688751.1:n.229-8C>G
ENST00000689792.1:n.997-8C>G
ENST00000262948.10:c.1093-8C>G MANE Select ENSP00000262948.4:n.1093-8C>G
ENST00000262948.9:c.1093-8C>G ENSP00000262948.3:n.1093-8C>G
ENST00000394867.8:c.802-8C>G ENSP00000378336.1:n.802-8C>G
ENST00000597263.5:n.278-8C>G
ENST00000599021.1:c.203-8C>G
ENST00000600584.5:n.2542-8C>G
ENST00000601786.5:n.1394-8C>G
NM_030662.3:c.1093-8C>G , LRG_750t1:c.1093-8C>G NP_109587.1:n.1093-8C>G
XM_006722799.2:c.814-8C>G XP_006722862.1:n.814-8C>G
XM_011528133.1:c.523-8C>G XP_011526435.1:n.523-8C>G
NM_030662.4:c.1093-8C>G MANE Select NP_109587.1:n.1093-8C>G
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