Canonical Allele Identifier: CA304447213

Gene: MAP2K2

Linked Data

• dbSNP Id: rs559885829
• gnomAD v3: 19-4094710-C-A
• gnomAD v4: 19-4094710-C-A
• MyVariant Identifiers: chr19:g.4094708C>A (hg19) ; chr19:g.4094710C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094710C>A , CM000681.2:g.4094710C>A	GRCh38
NC_000019.9:g.4094708C>A , CM000681.1:g.4094708C>A	GRCh37
NC_000019.8:g.4045708C>A	NCBI36
NG_007996.1:g.34419G>T , LRG_750:g.34419G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-212G>T
ENST00000688002.1:n.3198-212G>T
ENST00000688751.1:n.183-212G>T
ENST00000689792.1:n.951-212G>T
ENST00000262948.10:c.1047-212G>T MANE Select	ENSP00000262948.4:n.1047-212G>T
ENST00000262948.9:c.1047-212G>T	ENSP00000262948.3:n.1047-212G>T
ENST00000394867.8:c.756-212G>T	ENSP00000378336.1:n.756-212G>T
ENST00000597263.5:n.232-212G>T
ENST00000599021.1:c.157-212G>T
ENST00000600584.5:n.2284G>T
ENST00000601786.5:n.1348-212G>T
NM_030662.3:c.1047-212G>T , LRG_750t1:c.1047-212G>T	NP_109587.1:n.1047-212G>T
XM_006722799.2:c.768-212G>T	XP_006722862.1:n.768-212G>T
XM_011528133.1:c.477-212G>T	XP_011526435.1:n.477-212G>T
XM_017026989.1:c.1383G>T	XP_016882478.1:p.Gly461=
XM_017026990.1:c.1104G>T	XP_016882479.1:p.Gly368=
NM_030662.4:c.1047-212G>T MANE Select	NP_109587.1:n.1047-212G>T