Canonical Allele Identifier: CA2789273800
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837454C>G , CM000672.2:g.102837454C>G GRCh38
NC_000010.10:g.104597211C>G , CM000672.1:g.104597211C>G GRCh37
NC_000010.9:g.104587201C>G NCBI36
NG_007955.1:g.5080G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638190.1:c.-93G>C ENSP00000492539.1:n.-93G>C
ENST00000638971.1:c.-93G>C ENSP00000492313.1:n.-93G>C
ENST00000369887.3:c.-93G>C ENSP00000358903.3:n.-93G>C
NM_000102.3:c.-93G>C NP_000093.1:n.-93G>C