Canonical Allele Identifier: CA1192293650
Gene: HSD3B2 HGNC NCBI

Linked Data

dbSNP Id: rs1057504555
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119422821C>G , CM000663.2:g.119422821C>G GRCh38
NC_000001.10:g.119965444C>G , CM000663.1:g.119965444C>G GRCh37
NC_000001.9:g.119766967C>G NCBI36
NG_013349.1:g.12891C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369416.4:c.*201C>G MANE Select ENSP00000358424.3:n.*201C>G
ENST00000369416.3:c.*201C>G ENSP00000358424.3:n.*201C>G
ENST00000543831.5:c.*201C>G ENSP00000445122.1:n.*201C>G
NM_000198.3:c.*201C>G NP_000189.1:n.*201C>G
NM_001166120.1:c.*201C>G NP_001159592.1:n.*201C>G
NM_000198.4:c.*201C>G MANE Select NP_000189.1:n.*201C>G
NM_001166120.2:c.*201C>G NP_001159592.1:n.*201C>G
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