Canonical Allele Identifier: CA504984309
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090622-G-T
MyVariant Identifiers: chr19:g.4090620G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090622G>T , CM000681.2:g.4090622G>T GRCh38
NC_000019.9:g.4090620G>T , CM000681.1:g.4090620G>T GRCh37
NC_000019.8:g.4041620G>T NCBI36
NG_007996.1:g.38507C>A , LRG_750:g.38507C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1618C>A
ENST00000688002.1:n.3330C>A
ENST00000688751.1:n.315C>A
ENST00000689792.1:n.1083C>A
ENST00000262948.10:c.1179C>A MANE Select ENSP00000262948.4:p.Gly393=
ENST00000262948.9:c.1179C>A ENSP00000262948.3:p.Gly393=
ENST00000394867.8:c.888C>A ENSP00000378336.1:p.Gly296=
ENST00000597263.5:n.364C>A
ENST00000599021.1:c.289C>A
ENST00000600584.5:n.2628C>A
ENST00000601786.5:n.1480C>A
NM_030662.3:c.1179C>A , LRG_750t1:c.1179C>A NP_109587.1:p.Gly393=
XM_006722799.2:c.900C>A XP_006722862.1:p.Gly300=
XM_011528133.1:c.609C>A XP_011526435.1:p.Gly203=
NM_030662.4:c.1179C>A MANE Select NP_109587.1:p.Gly393=