Canonical Allele Identifier: CA346597856

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1241588085
• gnomAD v3: 2-31529314-G-A
• gnomAD v4: 2-31529314-G-A
• MyVariant Identifiers: chr2:g.31754384G>A (hg19) ; chr2:g.31529314G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529314G>A , CM000664.2:g.31529314G>A	GRCh38
NC_000002.11:g.31754384G>A , CM000664.1:g.31754384G>A	GRCh37
NC_000002.10:g.31607888G>A	NCBI36
NG_008365.1:g.56658C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.691C>T MANE Select	ENSP00000477587.1:p.His231Tyr
ENST00000622030.1:c.691C>T	ENSP00000477587.1:p.His231Tyr
NM_000348.3:c.691C>T	NP_000339.2:p.His231Tyr
XM_011533069.1:c.469C>T	XP_011531371.1:p.His157Tyr
XM_011533070.1:c.436C>T	XP_011531372.1:p.His146Tyr
XM_011533071.1:c.436C>T	XP_011531373.1:p.His146Tyr
XM_011533072.1:c.436C>T	XP_011531374.1:p.His146Tyr
XM_011533069.2:c.469C>T	XP_011531371.1:p.His157Tyr
XM_011533072.2:c.436C>T	XP_011531374.1:p.His146Tyr
NM_000348.4:c.691C>T MANE Select	NP_000339.2:p.His231Tyr