Canonical Allele Identifier: CA420187454
Gene: HSD3B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.119964874T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119422251T>G , CM000663.2:g.119422251T>G GRCh38
NC_000001.10:g.119964874T>G , CM000663.1:g.119964874T>G GRCh37
NC_000001.9:g.119766397T>G NCBI36
NG_013349.1:g.12321T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369416.4:c.750T>G MANE Select ENSP00000358424.3:p.Gly250=
ENST00000369416.3:c.750T>G ENSP00000358424.3:p.Gly250=
ENST00000543831.5:c.750T>G ENSP00000445122.1:p.Gly250=
NM_000198.3:c.750T>G NP_000189.1:p.Gly250=
NM_001166120.1:c.750T>G NP_001159592.1:p.Gly250=
NM_000198.4:c.750T>G MANE Select NP_000189.1:p.Gly250=
NM_001166120.2:c.750T>G NP_001159592.1:p.Gly250=