Canonical Allele Identifier: CA11062378
Gene: SRD5A2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3731586

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31523958T>C , CM000664.2:g.31523958T>C GRCh38
NC_000002.11:g.31749028T>C , CM000664.1:g.31749028T>C GRCh37
NC_000002.10:g.31602532T>C NCBI36
NG_008365.1:g.62014A>G

Transcript Alleles

HGVS Amino-acid change
XM_011533069.1:c.*2238A>G XP_011531371.1:p.=
XM_011533070.1:c.*2238A>G XP_011531372.1:p.=
XM_011533071.1:c.*2238A>G XP_011531373.1:p.=
XM_011533072.1:c.*2238A>G XP_011531374.1:p.=
XM_011533069.2:c.*2238A>G XP_011531371.1:p.=
XM_011533072.2:c.*2238A>G XP_011531374.1:p.=
NM_000348.4:c.*2238A>G VV MANE Preferred NP_000339.2:p.=
ENST00000622030.1:c.*2238A>G ENSP00000477587.1:p.=