Canonical Allele Identifier: CA195538327
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs895696659
MyVariant Identifiers: chr9:g.88693322T>C (hg19) chr9:g.86078407T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078407T>C , CM000671.2:g.86078407T>C GRCh38
NC_000009.11:g.88693322T>C , CM000671.1:g.88693322T>C GRCh37
NC_000009.10:g.87883142T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.129+785A>G ENSP00000373363.3:n.129+785A>G
ENST00000388712.7:c.129+785A>G MANE Select ENSP00000373364.3:n.129+785A>G
ENST00000466178.1:c.129+785A>G ENSP00000418155.1:n.129+785A>G
ENST00000470762.6:c.129+785A>G ENSP00000417504.2:n.129+785A>G
ENST00000472919.1:n.191-868A>G
ENST00000486130.5:c.129+785A>G ENSP00000419076.1:n.129+785A>G
NM_016548.3:c.129+785A>G NP_057632.2:n.129+785A>G
NM_177937.2:c.129+785A>G NP_808800.1:n.129+785A>G
NM_016548.4:c.129+785A>G MANE Select NP_057632.2:n.129+785A>G
NM_177937.3:c.129+785A>G NP_808800.1:n.129+785A>G
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