Canonical Allele Identifier: CA588729096
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1202178311
gnomAD v2: 9-88699917-G-A
gnomAD v3: 9-86085002-G-A
gnomAD v4: 9-86085002-G-A
MyVariant Identifiers: chr9:g.88699917G>A (hg19) chr9:g.86085002G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86085002G>A , CM000671.2:g.86085002G>A GRCh38
NC_000009.11:g.88699917G>A , CM000671.1:g.88699917G>A GRCh37
NC_000009.10:g.87889737G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5661C>T ENSP00000373363.3:n.-21-5661C>T
ENST00000388712.7:c.-21-5661C>T MANE Select ENSP00000373364.3:n.-21-5661C>T
ENST00000466178.1:c.-104C>T ENSP00000418155.1:n.-104C>T
ENST00000472919.1:n.150-5661C>T
NM_016548.3:c.-21-5661C>T NP_057632.2:n.-21-5661C>T
NM_177937.2:c.-21-5661C>T NP_808800.1:n.-21-5661C>T
NM_016548.4:c.-21-5661C>T MANE Select NP_057632.2:n.-21-5661C>T
NM_177937.3:c.-21-5661C>T NP_808800.1:n.-21-5661C>T
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