Canonical Allele Identifier: CA2585249253

Gene: MAP2K2

Linked Data

• dbSNP Id: rs529263334
• gnomAD v4: 19-4110468-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4110468C>G , CM000681.2:g.4110468C>G	GRCh38
NC_000019.9:g.4110466C>G , CM000681.1:g.4110466C>G	GRCh37
NC_000019.8:g.4061466C>G	NCBI36
NG_007996.1:g.18661G>C , LRG_750:g.18661G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.889+41G>C
ENST00000687128.1:n.889+41G>C
ENST00000262948.10:c.450+41G>C MANE Select	ENSP00000262948.4:n.450+41G>C
ENST00000262948.9:c.450+41G>C	ENSP00000262948.3:n.450+41G>C
ENST00000394867.8:c.159+41G>C	ENSP00000378336.1:n.159+41G>C
ENST00000599345.1:n.647+41G>C
NM_030662.3:c.450+41G>C , LRG_750t1:c.450+41G>C	NP_109587.1:n.450+41G>C
XM_006722799.2:c.450+41G>C	XP_006722862.1:n.450+41G>C
XM_017026989.1:c.450+41G>C	XP_016882478.1:n.450+41G>C
XM_017026990.1:c.450+41G>C	XP_016882479.1:n.450+41G>C
XM_017026991.1:c.450+41G>C	XP_016882480.1:n.450+41G>C
NM_030662.4:c.450+41G>C MANE Select	NP_109587.1:n.450+41G>C