Canonical Allele Identifier: CA346597789

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31751316A>C (hg19) ; chr2:g.31526246A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526246A>C , CM000664.2:g.31526246A>C	GRCh38
NC_000002.11:g.31751316A>C , CM000664.1:g.31751316A>C	GRCh37
NC_000002.10:g.31604820A>C	NCBI36
NG_008365.1:g.59726T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.715T>G MANE Select	ENSP00000477587.1:p.Phe239Val
ENST00000622030.1:c.715T>G	ENSP00000477587.1:p.Phe239Val
NM_000348.3:c.715T>G	NP_000339.2:p.Phe239Val
XM_011533069.1:c.493T>G	XP_011531371.1:p.Phe165Val
XM_011533070.1:c.460T>G	XP_011531372.1:p.Phe154Val
XM_011533071.1:c.460T>G	XP_011531373.1:p.Phe154Val
XM_011533072.1:c.460T>G	XP_011531374.1:p.Phe154Val
XM_011533069.2:c.493T>G	XP_011531371.1:p.Phe165Val
XM_011533072.2:c.460T>G	XP_011531374.1:p.Phe154Val
NM_000348.4:c.715T>G MANE Select	NP_000339.2:p.Phe239Val