Canonical Allele Identifier: CA346598381

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31756540C>A (hg19) ; chr2:g.31531470C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531470C>A , CM000664.2:g.31531470C>A	GRCh38
NC_000002.11:g.31756540C>A , CM000664.1:g.31756540C>A	GRCh37
NC_000002.10:g.31610044C>A	NCBI36
NG_008365.1:g.54502G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.448G>T MANE Select	ENSP00000477587.1:p.Val150Phe
ENST00000622030.1:c.448G>T	ENSP00000477587.1:p.Val150Phe
NM_000348.3:c.448G>T	NP_000339.2:p.Val150Phe
XM_011533069.1:c.226G>T	XP_011531371.1:p.Val76Phe
XM_011533070.1:c.193G>T	XP_011531372.1:p.Val65Phe
XM_011533071.1:c.193G>T	XP_011531373.1:p.Val65Phe
XM_011533072.1:c.193G>T	XP_011531374.1:p.Val65Phe
XM_011533069.2:c.226G>T	XP_011531371.1:p.Val76Phe
XM_011533072.2:c.193G>T	XP_011531374.1:p.Val65Phe
NM_000348.4:c.448G>T MANE Select	NP_000339.2:p.Val150Phe