Canonical Allele Identifier: CA304449331

Gene: MAP2K2

Linked Data

• dbSNP Id: rs778077063
• MyVariant Identifiers: chr19:g.4099393G>C (hg19) ; chr19:g.4099395G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099395G>C , CM000681.2:g.4099395G>C	GRCh38
NC_000019.9:g.4099393G>C , CM000681.1:g.4099393G>C	GRCh37
NC_000019.8:g.4050393G>C	NCBI36
NG_007996.1:g.29734C>G , LRG_750:g.29734C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1164C>G
ENST00000687128.1:n.1164C>G
ENST00000688002.1:n.1019C>G
ENST00000689792.1:n.646-17C>G
ENST00000262948.10:c.725C>G MANE Select	ENSP00000262948.4:p.Thr242Arg
ENST00000262948.9:c.725C>G	ENSP00000262948.3:p.Thr242Arg
ENST00000394867.8:c.434C>G	ENSP00000378336.1:p.Thr145Arg
ENST00000593364.5:n.672C>G
ENST00000595715.1:n.540C>G
ENST00000597263.5:n.169+1624C>G
ENST00000599021.1:c.29+1624C>G
ENST00000600584.5:n.1285C>G
ENST00000601786.5:n.1026C>G
NM_030662.3:c.725C>G , LRG_750t1:c.725C>G	NP_109587.1:p.Thr242Arg
XM_006722799.2:c.705+1624C>G	XP_006722862.1:n.705+1624C>G
XM_011528133.1:c.155C>G	XP_011526435.1:p.Thr52Arg
XM_017026989.1:c.725C>G	XP_016882478.1:p.Thr242Arg
XM_017026990.1:c.705+1624C>G	XP_016882479.1:n.705+1624C>G
NM_030662.4:c.725C>G MANE Select	NP_109587.1:p.Thr242Arg