Canonical Allele Identifier: CA341396066

Gene: HSD3B2

Linked Data

• MyVariant Identifiers: chr1:g.119964486A>T (hg19) ; chr1:g.119421863A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119421863A>T , CM000663.2:g.119421863A>T	GRCh38
NC_000001.10:g.119964486A>T , CM000663.1:g.119964486A>T	GRCh37
NC_000001.9:g.119766009A>T	NCBI36
NG_013349.1:g.11933A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369416.4:c.362A>T MANE Select	ENSP00000358424.3:p.Tyr121Phe
ENST00000369416.3:c.362A>T	ENSP00000358424.3:p.Tyr121Phe
ENST00000433745.5:c.362A>T	ENSP00000388292.1:p.Tyr121Phe
ENST00000448448.2:n.306A>T
ENST00000543831.5:c.362A>T	ENSP00000445122.1:p.Tyr121Phe
NM_000198.3:c.362A>T	NP_000189.1:p.Tyr121Phe
NM_001166120.1:c.362A>T	NP_001159592.1:p.Tyr121Phe
NM_000198.4:c.362A>T MANE Select	NP_000189.1:p.Tyr121Phe
NM_001166120.2:c.362A>T	NP_001159592.1:p.Tyr121Phe