Canonical Allele Identifier: CA1036079

Gene: HSD3B2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119422504C>T , CM000663.2:g.119422504C>T	GRCh38
NC_000001.10:g.119965127C>T , CM000663.1:g.119965127C>T	GRCh37
NC_000001.9:g.119766650C>T	NCBI36
NG_013349.1:g.12574C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000198.4:c.1003C>T MANE Select	NP_000189.1:p.Arg335Ter
ENST00000369416.4:c.1003C>T MANE Select	ENSP00000358424.3:p.Arg335Ter
NM_000198.3:c.1003C>T	NP_000189.1:p.Arg335Ter
NM_001166120.1:c.1003C>T	NP_001159592.1:p.Arg335Ter
NM_001166120.2:c.1003C>T	NP_001159592.1:p.Arg335Ter
ENST00000369416.3:c.1003C>T	ENSP00000358424.3:p.Arg335Ter
ENST00000543831.5:c.1003C>T	ENSP00000445122.1:p.Arg335Ter