Canonical Allele Identifier: CA304447516

Gene: MAP2K2

Linked Data

• dbSNP Id: rs587781029
• MyVariant Identifiers: chr19:g.4095373C>G (hg19) ; chr19:g.4095375C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095375C>G , CM000681.2:g.4095375C>G	GRCh38
NC_000019.9:g.4095373C>G , CM000681.1:g.4095373C>G	GRCh37
NC_000019.8:g.4046373C>G	NCBI36
NG_007996.1:g.33754G>C , LRG_750:g.33754G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485+13G>C
ENST00000688002.1:n.3197+13G>C
ENST00000688751.1:n.182+13G>C
ENST00000689792.1:n.950+13G>C
ENST00000262948.10:c.1046+13G>C MANE Select	ENSP00000262948.4:n.1046+13G>C
ENST00000262948.9:c.1046+13G>C	ENSP00000262948.3:n.1046+13G>C
ENST00000394867.8:c.755+13G>C	ENSP00000378336.1:n.755+13G>C
ENST00000597263.5:n.231+13G>C
ENST00000599021.1:c.156+13G>C
ENST00000600584.5:n.1619G>C
ENST00000601786.5:n.1347+13G>C
NM_030662.3:c.1046+13G>C , LRG_750t1:c.1046+13G>C	NP_109587.1:n.1046+13G>C
XM_006722799.2:c.767+13G>C	XP_006722862.1:n.767+13G>C
XM_011528133.1:c.476+13G>C	XP_011526435.1:n.476+13G>C
XM_017026989.1:c.1046+13G>C	XP_016882478.1:n.1046+13G>C
XM_017026990.1:c.767+13G>C	XP_016882479.1:n.767+13G>C
NM_030662.4:c.1046+13G>C MANE Select	NP_109587.1:n.1046+13G>C