Canonical Allele Identifier: CA11006412
Gene: SRD5A2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12470143

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31538488C>T , CM000664.2:g.31538488C>T GRCh38
NC_000002.11:g.31763558C>T , CM000664.1:g.31763558C>T GRCh37
NC_000002.10:g.31617062C>T NCBI36
NG_008365.1:g.47484G>A

Transcript Alleles

HGVS Amino-acid change
NM_000348.3:c.282-4722G>A VV NP_000339.2:p.=
XM_011533068.1:c.282-4722G>A XP_011531370.1:p.=
XM_011533069.1:c.60-4722G>A XP_011531371.1:p.=
XM_011533070.1:c.27-4722G>A XP_011531372.1:p.=
XM_011533071.1:c.27-4722G>A XP_011531373.1:p.=
XM_011533072.1:c.27-4722G>A XP_011531374.1:p.=
XM_011533069.2:c.60-4722G>A XP_011531371.1:p.=
XM_011533072.2:c.27-4722G>A XP_011531374.1:p.=
NM_000348.4:c.282-4722G>A VV MANE Preferred NP_000339.2:p.=
ENST00000622030.1:c.282-4722G>A ENSP00000477587.1:p.=