Canonical Allele Identifier: CA121935

Gene: HSD3B2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119422277C>T , CM000663.2:g.119422277C>T	GRCh38
NC_000001.10:g.119964900C>T , CM000663.1:g.119964900C>T	GRCh37
NC_000001.9:g.119766423C>T	NCBI36
NG_013349.1:g.12347C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000198.4:c.776C>T MANE Select	NP_000189.1:p.Thr259Met
ENST00000369416.4:c.776C>T MANE Select	ENSP00000358424.3:p.Thr259Met
NM_000198.3:c.776C>T	NP_000189.1:p.Thr259Met
NM_001166120.1:c.776C>T	NP_001159592.1:p.Thr259Met
NM_001166120.2:c.776C>T	NP_001159592.1:p.Thr259Met
ENST00000369416.3:c.776C>T	ENSP00000358424.3:p.Thr259Met
ENST00000543831.5:c.776C>T	ENSP00000445122.1:p.Thr259Met