Canonical Allele Identifier: CA882241841

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1216880035
• MyVariant Identifiers: chr19:g.4094671G>T (hg19) ; chr19:g.4094673G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094673G>T , CM000681.2:g.4094673G>T	GRCh38
NC_000019.9:g.4094671G>T , CM000681.1:g.4094671G>T	GRCh37
NC_000019.8:g.4045671G>T	NCBI36
NG_007996.1:g.34456C>A , LRG_750:g.34456C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-175C>A
ENST00000688002.1:n.3198-175C>A
ENST00000688751.1:n.183-175C>A
ENST00000689792.1:n.951-175C>A
ENST00000262948.10:c.1047-175C>A MANE Select	ENSP00000262948.4:n.1047-175C>A
ENST00000262948.9:c.1047-175C>A	ENSP00000262948.3:n.1047-175C>A
ENST00000394867.8:c.756-175C>A	ENSP00000378336.1:n.756-175C>A
ENST00000597263.5:n.232-175C>A
ENST00000599021.1:c.157-175C>A
ENST00000600584.5:n.2321C>A
ENST00000601786.5:n.1348-175C>A
NM_030662.3:c.1047-175C>A , LRG_750t1:c.1047-175C>A	NP_109587.1:n.1047-175C>A
XM_006722799.2:c.768-175C>A	XP_006722862.1:n.768-175C>A
XM_011528133.1:c.477-175C>A	XP_011526435.1:n.477-175C>A
XM_017026989.1:c.1420C>A	XP_016882478.1:p.Pro474Thr
XM_017026990.1:c.1141C>A	XP_016882479.1:p.Pro381Thr
NM_030662.4:c.1047-175C>A MANE Select	NP_109587.1:n.1047-175C>A