Canonical Allele Identifier: CA346598195
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531388C>G , CM000664.2:g.31531388C>G GRCh38
NC_000002.11:g.31756458C>G , CM000664.1:g.31756458C>G GRCh37
NC_000002.10:g.31609962C>G NCBI36
NG_008365.1:g.54584G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.530G>C MANE Select ENSP00000477587.1:p.Ser177Thr
ENST00000622030.1:c.530G>C ENSP00000477587.1:p.Ser177Thr
NM_000348.3:c.530G>C NP_000339.2:p.Ser177Thr
XM_011533069.1:c.308G>C XP_011531371.1:p.Ser103Thr
XM_011533070.1:c.275G>C XP_011531372.1:p.Ser92Thr
XM_011533071.1:c.275G>C XP_011531373.1:p.Ser92Thr
XM_011533072.1:c.275G>C XP_011531374.1:p.Ser92Thr
XM_011533069.2:c.308G>C XP_011531371.1:p.Ser103Thr
XM_011533072.2:c.275G>C XP_011531374.1:p.Ser92Thr
NM_000348.4:c.530G>C MANE Select NP_000339.2:p.Ser177Thr