Canonical Allele Identifier: CA1148185448
Gene: HSD3B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119422973T= , CM000663.2:g.119422973T= GRCh38
NC_000001.10:g.119965596T= , CM000663.1:g.119965596T= GRCh37
NC_000001.9:g.119767119T= NCBI36
NG_013349.1:g.13043T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369416.4:c.*353T= MANE Select ENSP00000358424.3:n.*353T=
ENST00000369416.3:c.*353T= ENSP00000358424.3:n.*353T=
ENST00000543831.5:c.*353T= ENSP00000445122.1:n.*353T=
NM_000198.3:c.*353T= NP_000189.1:n.*353T=
NM_001166120.1:c.*353T= NP_001159592.1:n.*353T=
NM_000198.4:c.*353T= MANE Select NP_000189.1:n.*353T=
NM_001166120.2:c.*353T= NP_001159592.1:n.*353T=
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