Canonical Allele Identifier: CA504984342
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090670-C-T
MyVariant Identifiers: chr19:g.4090668C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090670C>T , CM000681.2:g.4090670C>T GRCh38
NC_000019.9:g.4090668C>T , CM000681.1:g.4090668C>T GRCh37
NC_000019.8:g.4041668C>T NCBI36
NG_007996.1:g.38459G>A , LRG_750:g.38459G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1570G>A
ENST00000688002.1:n.3282G>A
ENST00000688751.1:n.267G>A
ENST00000689792.1:n.1035G>A
ENST00000262948.10:c.1131G>A MANE Select ENSP00000262948.4:p.Val377=
ENST00000262948.9:c.1131G>A ENSP00000262948.3:p.Val377=
ENST00000394867.8:c.840G>A ENSP00000378336.1:p.Val280=
ENST00000597263.5:n.316G>A
ENST00000599021.1:c.241G>A
ENST00000600584.5:n.2580G>A
ENST00000601786.5:n.1432G>A
NM_030662.3:c.1131G>A , LRG_750t1:c.1131G>A NP_109587.1:p.Val377=
XM_006722799.2:c.852G>A XP_006722862.1:p.Val284=
XM_011528133.1:c.561G>A XP_011526435.1:p.Val187=
NM_030662.4:c.1131G>A MANE Select NP_109587.1:p.Val377=