Canonical Allele Identifier: CA504984361
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090700-G-T
MyVariant Identifiers: chr19:g.4090698G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090700G>T , CM000681.2:g.4090700G>T GRCh38
NC_000019.9:g.4090698G>T , CM000681.1:g.4090698G>T GRCh37
NC_000019.8:g.4041698G>T NCBI36
NG_007996.1:g.38429C>A , LRG_750:g.38429C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1540C>A
ENST00000688002.1:n.3252C>A
ENST00000688751.1:n.237C>A
ENST00000689792.1:n.1005C>A
ENST00000262948.10:c.1101C>A MANE Select ENSP00000262948.4:p.Thr367=
ENST00000262948.9:c.1101C>A ENSP00000262948.3:p.Thr367=
ENST00000394867.8:c.810C>A ENSP00000378336.1:p.Thr270=
ENST00000597263.5:n.286C>A
ENST00000599021.1:c.211C>A
ENST00000600584.5:n.2550C>A
ENST00000601786.5:n.1402C>A
NM_030662.3:c.1101C>A , LRG_750t1:c.1101C>A NP_109587.1:p.Thr367=
XM_006722799.2:c.822C>A XP_006722862.1:p.Thr274=
XM_011528133.1:c.531C>A XP_011526435.1:p.Thr177=
NM_030662.4:c.1101C>A MANE Select NP_109587.1:p.Thr367=