Canonical Allele Identifier: CA867916174
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1191306529
MyVariant Identifiers: chr9:g.88693396A>T (hg19) chr9:g.86078481A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078481A>T , CM000671.2:g.86078481A>T GRCh38
NC_000009.11:g.88693396A>T , CM000671.1:g.88693396A>T GRCh37
NC_000009.10:g.87883216A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.129+711T>A ENSP00000373363.3:n.129+711T>A
ENST00000388712.7:c.129+711T>A MANE Select ENSP00000373364.3:n.129+711T>A
ENST00000466178.1:c.129+711T>A ENSP00000418155.1:n.129+711T>A
ENST00000470762.6:c.129+711T>A ENSP00000417504.2:n.129+711T>A
ENST00000472919.1:n.190+820T>A
ENST00000486130.5:c.129+711T>A ENSP00000419076.1:n.129+711T>A
NM_016548.3:c.129+711T>A NP_057632.2:n.129+711T>A
NM_177937.2:c.129+711T>A NP_808800.1:n.129+711T>A
NM_016548.4:c.129+711T>A MANE Select NP_057632.2:n.129+711T>A
NM_177937.3:c.129+711T>A NP_808800.1:n.129+711T>A
Search 100 bp 5'
Search 100 bp 3'