Canonical Allele Identifier: CA403385083

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145049465
• MyVariant Identifiers: chr19:g.4099197A>C (hg19) ; chr19:g.4099199A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099199A>C , CM000681.2:g.4099199A>C	GRCh38
NC_000019.9:g.4099197A>C , CM000681.1:g.4099197A>C	GRCh37
NC_000019.8:g.4050197A>C	NCBI36
NG_007996.1:g.29930T>G , LRG_750:g.29930T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+2T>G
ENST00000687128.1:n.1360T>G
ENST00000688002.1:n.1215T>G
ENST00000689792.1:n.823+2T>G
ENST00000262948.10:c.919+2T>G MANE Select	ENSP00000262948.4:n.919+2T>G
ENST00000262948.9:c.919+2T>G	ENSP00000262948.3:n.919+2T>G
ENST00000394867.8:c.628+2T>G	ENSP00000378336.1:n.628+2T>G
ENST00000593364.5:n.868T>G
ENST00000595715.1:n.734+2T>G
ENST00000597263.5:n.169+1820T>G
ENST00000599021.1:c.29+1820T>G
ENST00000600584.5:n.1479+2T>G
ENST00000601786.5:n.1220+2T>G
NM_030662.3:c.919+2T>G , LRG_750t1:c.919+2T>G	NP_109587.1:n.919+2T>G
XM_006722799.2:c.705+1820T>G	XP_006722862.1:n.705+1820T>G
XM_011528133.1:c.349+2T>G	XP_011526435.1:n.349+2T>G
XM_017026989.1:c.919+2T>G	XP_016882478.1:n.919+2T>G
XM_017026990.1:c.705+1820T>G	XP_016882479.1:n.705+1820T>G
NM_030662.4:c.919+2T>G MANE Select	NP_109587.1:n.919+2T>G