Canonical Allele Identifier: CA12991068
Gene: GOLM1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10868366

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86085145G>T , CM000671.2:g.86085145G>T GRCh38
NC_000009.10:g.87889880G>T NCBI36
NC_000009.11:g.88700060G>T , CM000671.1:g.88700060G>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5804C>A ENSP00000373363.3:p.=
ENST00000388712.7:c.-21-5804C>A ENSP00000373364.3:p.=
ENST00000466178.1:c.-141-106C>A ENSP00000418155.1:p.=
ENST00000472919.1:n.150-5804C>A
NM_016548.3:c.-21-5804C>A VV NP_057632.2:p.=
NM_177937.2:c.-21-5804C>A VV NP_808800.1:p.=