Canonical Allele Identifier: CA504984356
Gene: MAP2K2 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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