Canonical Allele Identifier: CA867920585
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1350228731
MyVariant Identifiers: chr9:g.88699995A>G (hg19) chr9:g.86085080A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86085080A>G , CM000671.2:g.86085080A>G GRCh38
NC_000009.11:g.88699995A>G , CM000671.1:g.88699995A>G GRCh37
NC_000009.10:g.87889815A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5739T>C ENSP00000373363.3:n.-21-5739T>C
ENST00000388712.7:c.-21-5739T>C MANE Select ENSP00000373364.3:n.-21-5739T>C
ENST00000466178.1:c.-141-41T>C ENSP00000418155.1:n.-141-41T>C
ENST00000472919.1:n.150-5739T>C
NM_016548.3:c.-21-5739T>C NP_057632.2:n.-21-5739T>C
NM_177937.2:c.-21-5739T>C NP_808800.1:n.-21-5739T>C
NM_016548.4:c.-21-5739T>C MANE Select NP_057632.2:n.-21-5739T>C
NM_177937.3:c.-21-5739T>C NP_808800.1:n.-21-5739T>C
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