Canonical Allele Identifier: CA504984306
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs375253105
MyVariant Identifiers: chr19:g.4090617T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090619T>G , CM000681.2:g.4090619T>G GRCh38
NC_000019.9:g.4090617T>G , CM000681.1:g.4090617T>G GRCh37
NC_000019.8:g.4041617T>G NCBI36
NG_007996.1:g.38510A>C , LRG_750:g.38510A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1621A>C
ENST00000688002.1:n.3333A>C
ENST00000688751.1:n.318A>C
ENST00000689792.1:n.1086A>C
ENST00000262948.10:c.1182A>C MANE Select ENSP00000262948.4:p.Thr394=
ENST00000262948.9:c.1182A>C ENSP00000262948.3:p.Thr394=
ENST00000394867.8:c.891A>C ENSP00000378336.1:p.Thr297=
ENST00000597263.5:n.367A>C
ENST00000599021.1:c.292A>C
ENST00000600584.5:n.2631A>C
ENST00000601786.5:n.1483A>C
NM_030662.3:c.1182A>C , LRG_750t1:c.1182A>C NP_109587.1:p.Thr394=
XM_006722799.2:c.903A>C XP_006722862.1:p.Thr301=
XM_011528133.1:c.612A>C XP_011526435.1:p.Thr204=
NM_030662.4:c.1182A>C MANE Select NP_109587.1:p.Thr394=