Canonical Allele Identifier: CA2610725924
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102837471-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837471T>C , CM000672.2:g.102837471T>C GRCh38
NC_000010.10:g.104597228T>C , CM000672.1:g.104597228T>C GRCh37
NC_000010.9:g.104587218T>C NCBI36
NG_007955.1:g.5063A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000638190.1:c.-110A>G ENSP00000492539.1:n.-110A>G
ENST00000638971.1:c.-110A>G ENSP00000492313.1:n.-110A>G
ENST00000369887.3:c.-110A>G ENSP00000358903.3:n.-110A>G
NM_000102.3:c.-110A>G NP_000093.1:n.-110A>G
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