Canonical Allele Identifier: CA882244298

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1347836239
• gnomAD v3: 19-4099535-A-G
• gnomAD v4: 19-4099535-A-G
• MyVariant Identifiers: chr19:g.4099533A>G (hg19) ; chr19:g.4099535A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099535A>G , CM000681.2:g.4099535A>G	GRCh38
NC_000019.9:g.4099533A>G , CM000681.1:g.4099533A>G	GRCh37
NC_000019.8:g.4050533A>G	NCBI36
NG_007996.1:g.29594T>C , LRG_750:g.29594T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-121T>C
ENST00000687128.1:n.1145-121T>C
ENST00000688002.1:n.879T>C
ENST00000689792.1:n.646-157T>C
ENST00000262948.10:c.706-121T>C MANE Select	ENSP00000262948.4:n.706-121T>C
ENST00000262948.9:c.706-121T>C	ENSP00000262948.3:n.706-121T>C
ENST00000394867.8:c.415-121T>C	ENSP00000378336.1:n.415-121T>C
ENST00000593364.5:n.653-121T>C
ENST00000595715.1:n.400T>C
ENST00000597263.5:n.169+1484T>C
ENST00000599021.1:c.29+1484T>C
ENST00000600584.5:n.1145T>C
ENST00000601786.5:n.1007-121T>C
ENST00000602167.5:n.426-121T>C
NM_030662.3:c.706-121T>C , LRG_750t1:c.706-121T>C	NP_109587.1:n.706-121T>C
XM_006722799.2:c.705+1484T>C	XP_006722862.1:n.705+1484T>C
XM_011528133.1:c.136-121T>C	XP_011526435.1:n.136-121T>C
XM_017026989.1:c.706-121T>C	XP_016882478.1:n.706-121T>C
XM_017026990.1:c.705+1484T>C	XP_016882479.1:n.705+1484T>C
XM_017026991.1:c.*195T>C	XP_016882480.1:n.*195T>C
NM_030662.4:c.706-121T>C MANE Select	NP_109587.1:n.706-121T>C