Canonical Allele Identifier: CA1242215066
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1666779172

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31568338G>A , CM000664.2:g.31568338G>A GRCh38
NC_000002.11:g.31793408G>A , CM000664.1:g.31793408G>A GRCh37
NC_000002.10:g.31646912G>A NCBI36
NG_008365.1:g.17634C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+12282C>T MANE Select ENSP00000477587.1:n.281+12282C>T
ENST00000622030.1:c.281+12282C>T ENSP00000477587.1:n.281+12282C>T
NM_000348.3:c.281+12282C>T NP_000339.2:n.281+12282C>T
XM_011533068.1:c.281+12282C>T XP_011531370.1:n.281+12282C>T
XM_011533070.1:c.27-34572C>T XP_011531372.1:n.27-34572C>T
XM_011533071.1:c.27-34572C>T XP_011531373.1:n.27-34572C>T
XM_011533072.1:c.27-34572C>T XP_011531374.1:n.27-34572C>T
XM_011533072.2:c.27-34572C>T XP_011531374.1:n.27-34572C>T
NM_000348.4:c.281+12282C>T MANE Select NP_000339.2:n.281+12282C>T