Canonical Allele Identifier: CA867920439
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1199350355
MyVariant Identifiers: chr9:g.88699790C>G (hg19) chr9:g.86084875C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86084875C>G , CM000671.2:g.86084875C>G GRCh38
NC_000009.11:g.88699790C>G , CM000671.1:g.88699790C>G GRCh37
NC_000009.10:g.87889610C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5534G>C ENSP00000373363.3:n.-21-5534G>C
ENST00000388712.7:c.-21-5534G>C MANE Select ENSP00000373364.3:n.-21-5534G>C
ENST00000466178.1:c.-22+45G>C ENSP00000418155.1:n.-22+45G>C
ENST00000472919.1:n.150-5534G>C
NM_016548.3:c.-21-5534G>C NP_057632.2:n.-21-5534G>C
NM_177937.2:c.-21-5534G>C NP_808800.1:n.-21-5534G>C
NM_016548.4:c.-21-5534G>C MANE Select NP_057632.2:n.-21-5534G>C
NM_177937.3:c.-21-5534G>C NP_808800.1:n.-21-5534G>C
Search 100 bp 5'
Search 100 bp 3'