Canonical Allele Identifier: CA505162302

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145079808
• MyVariant Identifiers: chr19:g.4117444T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117446T>C , CM000681.2:g.4117446T>C	GRCh38
NC_000019.9:g.4117444T>C , CM000681.1:g.4117444T>C	GRCh37
NC_000019.8:g.4068444T>C	NCBI36
NG_007996.1:g.11683A>G , LRG_750:g.11683A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.715A>G
ENST00000687128.1:n.715A>G
ENST00000262948.10:c.276A>G MANE Select	ENSP00000262948.4:p.Arg92=
ENST00000262948.9:c.276A>G	ENSP00000262948.3:p.Arg92=
ENST00000394867.8:c.-16A>G	ENSP00000378336.1:n.-16A>G
ENST00000599345.1:n.473A>G
NM_030662.3:c.276A>G , LRG_750t1:c.276A>G	NP_109587.1:p.Arg92=
XM_006722799.2:c.276A>G	XP_006722862.1:p.Arg92=
XM_017026989.1:c.276A>G	XP_016882478.1:p.Arg92=
XM_017026990.1:c.276A>G	XP_016882479.1:p.Arg92=
XM_017026991.1:c.276A>G	XP_016882480.1:p.Arg92=
NM_030662.4:c.276A>G MANE Select	NP_109587.1:p.Arg92=