Canonical Allele Identifier: CA403386550

Gene: MAP2K2

Linked Data

• dbSNP Id: rs730880522
• MyVariant Identifiers: chr19:g.4099331C>G (hg19) ; chr19:g.4099333C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099333C>G , CM000681.2:g.4099333C>G	GRCh38
NC_000019.9:g.4099331C>G , CM000681.1:g.4099331C>G	GRCh37
NC_000019.8:g.4050331C>G	NCBI36
NG_007996.1:g.29796G>C , LRG_750:g.29796G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1226G>C
ENST00000687128.1:n.1226G>C
ENST00000688002.1:n.1081G>C
ENST00000689792.1:n.691G>C
ENST00000262948.10:c.787G>C MANE Select	ENSP00000262948.4:p.Gly263Arg
ENST00000262948.9:c.787G>C	ENSP00000262948.3:p.Gly263Arg
ENST00000394867.8:c.496G>C	ENSP00000378336.1:p.Gly166Arg
ENST00000593364.5:n.734G>C
ENST00000595715.1:n.602G>C
ENST00000597263.5:n.169+1686G>C
ENST00000599021.1:c.29+1686G>C
ENST00000600584.5:n.1347G>C
ENST00000601786.5:n.1088G>C
NM_030662.3:c.787G>C , LRG_750t1:c.787G>C	NP_109587.1:p.Gly263Arg
XM_006722799.2:c.705+1686G>C	XP_006722862.1:n.705+1686G>C
XM_011528133.1:c.217G>C	XP_011526435.1:p.Gly73Arg
XM_017026989.1:c.787G>C	XP_016882478.1:p.Gly263Arg
XM_017026990.1:c.705+1686G>C	XP_016882479.1:n.705+1686G>C
NM_030662.4:c.787G>C MANE Select	NP_109587.1:p.Gly263Arg