Canonical Allele Identifier: CA504895095
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1096552
ClinVar RCV Id: RCV001417804
dbSNP Id: rs2144636249
MyVariant Identifiers: chr19:g.1398960C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398961C>T , CM000681.2:g.1398961C>T GRCh38
NC_000019.9:g.1398960C>T , CM000681.1:g.1398960C>T GRCh37
NC_000019.8:g.1349960C>T NCBI36
NG_009785.1:g.7593G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.525G>A MANE Select ENSP00000252288.1:p.Gly175=
ENST00000447102.8:c.525G>A ENSP00000403536.2:p.Gly175=
ENST00000591788.3:c.208G>A
ENST00000640164.1:n.358G>A
ENST00000640762.1:c.456G>A ENSP00000492031.1:p.Gly152=
ENST00000252288.6:c.525G>A ENSP00000252288.1:p.Gly175=
ENST00000447102.7:c.525G>A ENSP00000403536.2:p.Gly175=
ENST00000591788.2:c.210G>A ENSP00000466341.2:p.Gly70=
NM_000156.5:c.525G>A NP_000147.1:p.Gly175=
NM_138924.2:c.525G>A NP_620279.1:p.Gly175=
NM_000156.6:c.525G>A MANE Select NP_000147.1:p.Gly175=
NM_138924.3:c.525G>A NP_620279.1:p.Gly175=