Canonical Allele Identifier: CA1192293644
Gene: HSD3B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119422819A= , CM000663.2:g.119422819A= GRCh38
NC_000001.10:g.119965442A= , CM000663.1:g.119965442A= GRCh37
NC_000001.9:g.119766965A= NCBI36
NG_013349.1:g.12889A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369416.4:c.*199A= MANE Select ENSP00000358424.3:n.*199A=
ENST00000369416.3:c.*199A= ENSP00000358424.3:n.*199A=
ENST00000543831.5:c.*199A= ENSP00000445122.1:n.*199A=
NM_000198.3:c.*199A= NP_000189.1:n.*199A=
NM_001166120.1:c.*199A= NP_001159592.1:n.*199A=
NM_000198.4:c.*199A= MANE Select NP_000189.1:n.*199A=
NM_001166120.2:c.*199A= NP_001159592.1:n.*199A=
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