Canonical Allele Identifier: CA10649148
Gene: GPR179 HGNC NCBI

Linked Data

ClinVar Variation Id: 322958
ClinVar RCV Id: RCV000374147
dbSNP Id: rs886052893
MyVariant Identifiers: chr17:g.38325949A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38325949A>G , CM000679.2:g.38325949A>G GRCh38
NC_000017.9:g.33735358A>G NCBI36
NG_032655.2:g.22862T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000616987.5:c.*516T>C MANE Select ENSP00000483469.2:n.*516T>C
ENST00000616987.4:c.*516T>C ENSP00000483469.1:n.*516T>C
ENST00000621958.1:c.*516T>C ENSP00000480024.1:n.*516T>C
ENST00000622573.1:n.135-256T>C
NM_001004334.3:c.*516T>C NP_001004334.3:n.*516T>C
NM_001004334.4:c.*516T>C MANE Select NP_001004334.3:n.*516T>C
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