Canonical Allele Identifier: CA504987044

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1230589884
• MyVariant Identifiers: chr19:g.4099395G>A (hg19) ; chr19:g.4099397G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099397G>A , CM000681.2:g.4099397G>A	GRCh38
NC_000019.9:g.4099395G>A , CM000681.1:g.4099395G>A	GRCh37
NC_000019.8:g.4050395G>A	NCBI36
NG_007996.1:g.29732C>T , LRG_750:g.29732C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1162C>T
ENST00000687128.1:n.1162C>T
ENST00000688002.1:n.1017C>T
ENST00000689792.1:n.646-19C>T
ENST00000262948.10:c.723C>T MANE Select	ENSP00000262948.4:p.Gly241=
ENST00000262948.9:c.723C>T	ENSP00000262948.3:p.Gly241=
ENST00000394867.8:c.432C>T	ENSP00000378336.1:p.Gly144=
ENST00000593364.5:n.670C>T
ENST00000595715.1:n.538C>T
ENST00000597263.5:n.169+1622C>T
ENST00000599021.1:c.29+1622C>T
ENST00000600584.5:n.1283C>T
ENST00000601786.5:n.1024C>T
NM_030662.3:c.723C>T , LRG_750t1:c.723C>T	NP_109587.1:p.Gly241=
XM_006722799.2:c.705+1622C>T	XP_006722862.1:n.705+1622C>T
XM_011528133.1:c.153C>T	XP_011526435.1:p.Gly51=
XM_017026989.1:c.723C>T	XP_016882478.1:p.Gly241=
XM_017026990.1:c.705+1622C>T	XP_016882479.1:n.705+1622C>T
NM_030662.4:c.723C>T MANE Select	NP_109587.1:p.Gly241=