Canonical Allele Identifier: CA1192293820

Gene: HSD3B2

Linked Data

• dbSNP Id: rs1651938918

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119422976C>T , CM000663.2:g.119422976C>T	GRCh38
NC_000001.10:g.119965599C>T , CM000663.1:g.119965599C>T	GRCh37
NC_000001.9:g.119767122C>T	NCBI36
NG_013349.1:g.13046C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369416.4:c.*356C>T MANE Select	ENSP00000358424.3:n.*356C>T
ENST00000369416.3:c.*356C>T	ENSP00000358424.3:n.*356C>T
ENST00000543831.5:c.*356C>T	ENSP00000445122.1:n.*356C>T
NM_000198.3:c.*356C>T	NP_000189.1:n.*356C>T
NM_001166120.1:c.*356C>T	NP_001159592.1:n.*356C>T
NM_000198.4:c.*356C>T MANE Select	NP_000189.1:n.*356C>T
NM_001166120.2:c.*356C>T	NP_001159592.1:n.*356C>T