Canonical Allele Identifier: CA767779868
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1353011797

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31568336T>C , CM000664.2:g.31568336T>C GRCh38
NC_000002.11:g.31793406T>C , CM000664.1:g.31793406T>C GRCh37
NC_000002.10:g.31646910T>C NCBI36
NG_008365.1:g.17636A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+12284A>G MANE Select ENSP00000477587.1:n.281+12284A>G
ENST00000622030.1:c.281+12284A>G ENSP00000477587.1:n.281+12284A>G
NM_000348.3:c.281+12284A>G NP_000339.2:n.281+12284A>G
XM_011533068.1:c.281+12284A>G XP_011531370.1:n.281+12284A>G
XM_011533070.1:c.27-34570A>G XP_011531372.1:n.27-34570A>G
XM_011533071.1:c.27-34570A>G XP_011531373.1:n.27-34570A>G
XM_011533072.1:c.27-34570A>G XP_011531374.1:n.27-34570A>G
XM_011533072.2:c.27-34570A>G XP_011531374.1:n.27-34570A>G
NM_000348.4:c.281+12284A>G MANE Select NP_000339.2:n.281+12284A>G