Canonical Allele Identifier: CA867920432
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs891099623
MyVariant Identifiers: chr9:g.88699789C>T (hg19) chr9:g.86084874C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86084874C>T , CM000671.2:g.86084874C>T GRCh38
NC_000009.11:g.88699789C>T , CM000671.1:g.88699789C>T GRCh37
NC_000009.10:g.87889609C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5533G>A ENSP00000373363.3:n.-21-5533G>A
ENST00000388712.7:c.-21-5533G>A MANE Select ENSP00000373364.3:n.-21-5533G>A
ENST00000466178.1:c.-22+46G>A ENSP00000418155.1:n.-22+46G>A
ENST00000472919.1:n.150-5533G>A
NM_016548.3:c.-21-5533G>A NP_057632.2:n.-21-5533G>A
NM_177937.2:c.-21-5533G>A NP_808800.1:n.-21-5533G>A
NM_016548.4:c.-21-5533G>A MANE Select NP_057632.2:n.-21-5533G>A
NM_177937.3:c.-21-5533G>A NP_808800.1:n.-21-5533G>A
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