Canonical Allele Identifier: CA504984357
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090694-G-T
MyVariant Identifiers: chr19:g.4090692G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090694G>T , CM000681.2:g.4090694G>T GRCh38
NC_000019.9:g.4090692G>T , CM000681.1:g.4090692G>T GRCh37
NC_000019.8:g.4041692G>T NCBI36
NG_007996.1:g.38435C>A , LRG_750:g.38435C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1546C>A
ENST00000688002.1:n.3258C>A
ENST00000688751.1:n.243C>A
ENST00000689792.1:n.1011C>A
ENST00000262948.10:c.1107C>A MANE Select ENSP00000262948.4:p.Ile369=
ENST00000262948.9:c.1107C>A ENSP00000262948.3:p.Ile369=
ENST00000394867.8:c.816C>A ENSP00000378336.1:p.Ile272=
ENST00000597263.5:n.292C>A
ENST00000599021.1:c.217C>A
ENST00000600584.5:n.2556C>A
ENST00000601786.5:n.1408C>A
NM_030662.3:c.1107C>A , LRG_750t1:c.1107C>A NP_109587.1:p.Ile369=
XM_006722799.2:c.828C>A XP_006722862.1:p.Ile276=
XM_011528133.1:c.537C>A XP_011526435.1:p.Ile179=
NM_030662.4:c.1107C>A MANE Select NP_109587.1:p.Ile369=