Canonical Allele Identifier: CA504986220

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145049493
• MyVariant Identifiers: chr19:g.4099203G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099205G>C , CM000681.2:g.4099205G>C	GRCh38
NC_000019.9:g.4099203G>C , CM000681.1:g.4099203G>C	GRCh37
NC_000019.8:g.4050203G>C	NCBI36
NG_007996.1:g.29924C>G , LRG_750:g.29924C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1354C>G
ENST00000687128.1:n.1354C>G
ENST00000688002.1:n.1209C>G
ENST00000689792.1:n.819C>G
ENST00000262948.10:c.915C>G MANE Select	ENSP00000262948.4:p.Val305=
ENST00000262948.9:c.915C>G	ENSP00000262948.3:p.Val305=
ENST00000394867.8:c.624C>G	ENSP00000378336.1:p.Val208=
ENST00000593364.5:n.862C>G
ENST00000595715.1:n.730C>G
ENST00000597263.5:n.169+1814C>G
ENST00000599021.1:c.29+1814C>G
ENST00000600584.5:n.1475C>G
ENST00000601786.5:n.1216C>G
NM_030662.3:c.915C>G , LRG_750t1:c.915C>G	NP_109587.1:p.Val305=
XM_006722799.2:c.705+1814C>G	XP_006722862.1:n.705+1814C>G
XM_011528133.1:c.345C>G	XP_011526435.1:p.Val115=
XM_017026989.1:c.915C>G	XP_016882478.1:p.Val305=
XM_017026990.1:c.705+1814C>G	XP_016882479.1:n.705+1814C>G
NM_030662.4:c.915C>G MANE Select	NP_109587.1:p.Val305=