Canonical Allele Identifier: CA2610725906
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102837438-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837438C>G , CM000672.2:g.102837438C>G GRCh38
NC_000010.10:g.104597195C>G , CM000672.1:g.104597195C>G GRCh37
NC_000010.9:g.104587185C>G NCBI36
NG_007955.1:g.5096G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638190.1:c.-77G>C ENSP00000492539.1:n.-77G>C
ENST00000638971.1:c.-77G>C ENSP00000492313.1:n.-77G>C
ENST00000369887.3:c.-77G>C ENSP00000358903.3:n.-77G>C
NM_000102.3:c.-77G>C NP_000093.1:n.-77G>C
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