Canonical Allele Identifier: CA403391430
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs2145069852

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4110565C>T , CM000681.2:g.4110565C>T GRCh38
NC_000019.9:g.4110563C>T , CM000681.1:g.4110563C>T GRCh37
NC_000019.8:g.4061563C>T NCBI36
NG_007996.1:g.18564G>A , LRG_750:g.18564G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.833G>A
ENST00000687128.1:n.833G>A
ENST00000262948.10:c.394G>A MANE Select ENSP00000262948.4:p.Gly132Ser
ENST00000262948.9:c.394G>A ENSP00000262948.3:p.Gly132Ser
ENST00000394867.8:c.103G>A ENSP00000378336.1:p.Gly35Ser
ENST00000599345.1:n.591G>A
NM_030662.3:c.394G>A , LRG_750t1:c.394G>A NP_109587.1:p.Gly132Ser
XM_006722799.2:c.394G>A XP_006722862.1:p.Gly132Ser
XM_017026989.1:c.394G>A XP_016882478.1:p.Gly132Ser
XM_017026990.1:c.394G>A XP_016882479.1:p.Gly132Ser
XM_017026991.1:c.394G>A XP_016882480.1:p.Gly132Ser
NM_030662.4:c.394G>A MANE Select NP_109587.1:p.Gly132Ser