Canonical Allele Identifier: CA304447007

Gene: MAP2K2

Linked Data

• dbSNP Id: rs929356112
• gnomAD v2: 19-4094241-C-T
• gnomAD v3: 19-4094243-C-T
• gnomAD v4: 19-4094243-C-T
• MyVariant Identifiers: chr19:g.4094241C>T (hg19) ; chr19:g.4094243C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094243C>T , CM000681.2:g.4094243C>T	GRCh38
NC_000019.9:g.4094241C>T , CM000681.1:g.4094241C>T	GRCh37
NC_000019.8:g.4045241C>T	NCBI36
NG_007996.1:g.34886G>A , LRG_750:g.34886G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1531+210G>A
ENST00000688002.1:n.3243+210G>A
ENST00000688751.1:n.228+210G>A
ENST00000689792.1:n.996+210G>A
ENST00000262948.10:c.1092+210G>A MANE Select	ENSP00000262948.4:n.1092+210G>A
ENST00000262948.9:c.1092+210G>A	ENSP00000262948.3:n.1092+210G>A
ENST00000394867.8:c.801+210G>A	ENSP00000378336.1:n.801+210G>A
ENST00000597263.5:n.277+210G>A
ENST00000599021.1:c.202+210G>A
ENST00000600584.5:n.2541+210G>A
ENST00000601786.5:n.1393+210G>A
NM_030662.3:c.1092+210G>A , LRG_750t1:c.1092+210G>A	NP_109587.1:n.1092+210G>A
XM_006722799.2:c.813+210G>A	XP_006722862.1:n.813+210G>A
XM_011528133.1:c.522+210G>A	XP_011526435.1:n.522+210G>A
NM_030662.4:c.1092+210G>A MANE Select	NP_109587.1:n.1092+210G>A