Canonical Allele Identifier: CA15155376
Gene: CYP20A1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11888559

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203300448T>C , CM000664.2:g.203300448T>C GRCh38
NC_000002.10:g.203873416T>C NCBI36
NC_000002.11:g.204165171T>C , CM000664.1:g.204165171T>C GRCh37
NG_007956.1:g.67008T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000611416.4:c.*3540T>C ENSP00000477866.1:p.=
ENST00000613925.4:c.*380+3160T>C ENSP00000482757.1:p.=
NM_177538.2:c.*3540T>C VV NP_803882.1:p.=