Canonical Allele Identifier: CA11224258
Gene: SRD5A2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11675297

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31568349G>A , CM000664.2:g.31568349G>A GRCh38
NC_000002.11:g.31793419G>A , CM000664.1:g.31793419G>A GRCh37
NC_000002.10:g.31646923G>A NCBI36
NG_008365.1:g.17623C>T

Transcript Alleles

HGVS Amino-acid change
NM_000348.3:c.281+12271C>T VV NP_000339.2:p.=
XM_011533068.1:c.281+12271C>T XP_011531370.1:p.=
XM_011533070.1:c.27-34583C>T XP_011531372.1:p.=
XM_011533071.1:c.27-34583C>T XP_011531373.1:p.=
XM_011533072.1:c.27-34583C>T XP_011531374.1:p.=
XM_011533072.2:c.27-34583C>T XP_011531374.1:p.=
NM_000348.4:c.281+12271C>T VV MANE Preferred NP_000339.2:p.=
ENST00000622030.1:c.281+12271C>T ENSP00000477587.1:p.=