Canonical Allele Identifier: CA403381279
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090708T>G (hg19) chr19:g.4090710T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090710T>G , CM000681.2:g.4090710T>G GRCh38
NC_000019.9:g.4090708T>G , CM000681.1:g.4090708T>G GRCh37
NC_000019.8:g.4041708T>G NCBI36
NG_007996.1:g.38419A>C , LRG_750:g.38419A>C

Transcript Alleles

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