Canonical Allele Identifier: CA304445658

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1038534034
• gnomAD v4: 19-4090514-C-T
• MyVariant Identifiers: chr19:g.4090512C>T (hg19) ; chr19:g.4090514C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090514C>T , CM000681.2:g.4090514C>T	GRCh38
NC_000019.9:g.4090512C>T , CM000681.1:g.4090512C>T	GRCh37
NC_000019.8:g.4041512C>T	NCBI36
NG_007996.1:g.38615G>A , LRG_750:g.38615G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1726G>A
ENST00000688002.1:n.3438G>A
ENST00000688751.1:n.423G>A
ENST00000689792.1:n.1191G>A
ENST00000262948.10:c.*84G>A MANE Select	ENSP00000262948.4:n.*84G>A
ENST00000262948.9:c.*84G>A	ENSP00000262948.3:n.*84G>A
ENST00000394867.8:c.*84G>A	ENSP00000378336.1:n.*84G>A
ENST00000597263.5:n.472G>A
ENST00000600584.5:n.2736G>A
ENST00000601786.5:n.1588G>A
NM_030662.3:c.*84G>A , LRG_750t1:c.*84G>A	NP_109587.1:n.*84G>A
XM_006722799.2:c.*84G>A	XP_006722862.1:n.*84G>A
XM_011528133.1:c.*84G>A	XP_011526435.1:n.*84G>A
NM_030662.4:c.*84G>A MANE Select	NP_109587.1:n.*84G>A