Canonical Allele Identifier: CA304456484

Gene: MAP2K2

Linked Data

• dbSNP Id: rs769010553
• gnomAD v2: 19-4117358-C-T
• gnomAD v3: 19-4117360-C-T
• gnomAD v4: 19-4117360-C-T
• MyVariant Identifiers: chr19:g.4117358C>T (hg19) ; chr19:g.4117360C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117360C>T , CM000681.2:g.4117360C>T	GRCh38
NC_000019.9:g.4117358C>T , CM000681.1:g.4117358C>T	GRCh37
NC_000019.8:g.4068358C>T	NCBI36
NG_007996.1:g.11769G>A , LRG_750:g.11769G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.742+59G>A
ENST00000687128.1:n.742+59G>A
ENST00000262948.10:c.303+59G>A MANE Select	ENSP00000262948.4:n.303+59G>A
ENST00000262948.9:c.303+59G>A	ENSP00000262948.3:n.303+59G>A
ENST00000394867.8:c.12+59G>A	ENSP00000378336.1:n.12+59G>A
ENST00000599345.1:n.500+59G>A
NM_030662.3:c.303+59G>A , LRG_750t1:c.303+59G>A	NP_109587.1:n.303+59G>A
XM_006722799.2:c.303+59G>A	XP_006722862.1:n.303+59G>A
XM_017026989.1:c.303+59G>A	XP_016882478.1:n.303+59G>A
XM_017026990.1:c.303+59G>A	XP_016882479.1:n.303+59G>A
XM_017026991.1:c.303+59G>A	XP_016882480.1:n.303+59G>A
NM_030662.4:c.303+59G>A MANE Select	NP_109587.1:n.303+59G>A