Canonical Allele Identifier: CA2319219800
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs571595941
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090727C>G , CM000681.2:g.4090727C>G GRCh38
NC_000019.9:g.4090725C>G , CM000681.1:g.4090725C>G GRCh37
NC_000019.8:g.4041725C>G NCBI36
NG_007996.1:g.38402G>C , LRG_750:g.38402G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-19G>C
ENST00000688002.1:n.3244-19G>C
ENST00000688751.1:n.229-19G>C
ENST00000689792.1:n.997-19G>C
ENST00000262948.10:c.1093-19G>C MANE Select ENSP00000262948.4:n.1093-19G>C
ENST00000262948.9:c.1093-19G>C ENSP00000262948.3:n.1093-19G>C
ENST00000394867.8:c.802-19G>C ENSP00000378336.1:n.802-19G>C
ENST00000597263.5:n.278-19G>C
ENST00000599021.1:c.203-19G>C
ENST00000600584.5:n.2542-19G>C
ENST00000601786.5:n.1394-19G>C
NM_030662.3:c.1093-19G>C , LRG_750t1:c.1093-19G>C NP_109587.1:n.1093-19G>C
XM_006722799.2:c.814-19G>C XP_006722862.1:n.814-19G>C
XM_011528133.1:c.523-19G>C XP_011526435.1:n.523-19G>C
NM_030662.4:c.1093-19G>C MANE Select NP_109587.1:n.1093-19G>C
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