Canonical Allele Identifier: CA2735341530

Gene: MAP2K2

Linked Data

• dbSNP Id: rs750109603

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117684G>C , CM000681.2:g.4117684G>C	GRCh38
NC_000019.9:g.4117682G>C , CM000681.1:g.4117682G>C	GRCh37
NC_000019.8:g.4068682G>C	NCBI36
NG_007996.1:g.11445C>G , LRG_750:g.11445C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.477C>G
ENST00000687128.1:n.477C>G
ENST00000262948.10:c.93-55C>G MANE Select	ENSP00000262948.4:n.93-55C>G
ENST00000262948.9:c.93-55C>G	ENSP00000262948.3:n.93-55C>G
ENST00000394867.8:c.-199-55C>G	ENSP00000378336.1:n.-199-55C>G
ENST00000599345.1:n.290-55C>G
NM_030662.3:c.93-55C>G , LRG_750t1:c.93-55C>G	NP_109587.1:n.93-55C>G
XM_006722799.2:c.93-55C>G	XP_006722862.1:n.93-55C>G
XM_017026989.1:c.93-55C>G	XP_016882478.1:n.93-55C>G
XM_017026990.1:c.93-55C>G	XP_016882479.1:n.93-55C>G
XM_017026991.1:c.93-55C>G	XP_016882480.1:n.93-55C>G
NM_030662.4:c.93-55C>G MANE Select	NP_109587.1:n.93-55C>G