Canonical Allele Identifier: CA346597885

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31754399G>T (hg19) ; chr2:g.31529329G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529329G>T , CM000664.2:g.31529329G>T	GRCh38
NC_000002.11:g.31754399G>T , CM000664.1:g.31754399G>T	GRCh37
NC_000002.10:g.31607903G>T	NCBI36
NG_008365.1:g.56643C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.676C>A MANE Select	ENSP00000477587.1:p.Leu226Met
ENST00000622030.1:c.676C>A	ENSP00000477587.1:p.Leu226Met
NM_000348.3:c.676C>A	NP_000339.2:p.Leu226Met
XM_011533069.1:c.454C>A	XP_011531371.1:p.Leu152Met
XM_011533070.1:c.421C>A	XP_011531372.1:p.Leu141Met
XM_011533071.1:c.421C>A	XP_011531373.1:p.Leu141Met
XM_011533072.1:c.421C>A	XP_011531374.1:p.Leu141Met
XM_011533069.2:c.454C>A	XP_011531371.1:p.Leu152Met
XM_011533072.2:c.421C>A	XP_011531374.1:p.Leu141Met
NM_000348.4:c.676C>A MANE Select	NP_000339.2:p.Leu226Met