Canonical Allele Identifier: CA346598173
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531379A>C , CM000664.2:g.31531379A>C GRCh38
NC_000002.11:g.31756449A>C , CM000664.1:g.31756449A>C GRCh37
NC_000002.10:g.31609953A>C NCBI36
NG_008365.1:g.54593T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.539T>G MANE Select ENSP00000477587.1:p.Ile180Ser
ENST00000622030.1:c.539T>G ENSP00000477587.1:p.Ile180Ser
NM_000348.3:c.539T>G NP_000339.2:p.Ile180Ser
XM_011533069.1:c.317T>G XP_011531371.1:p.Ile106Ser
XM_011533070.1:c.284T>G XP_011531372.1:p.Ile95Ser
XM_011533071.1:c.284T>G XP_011531373.1:p.Ile95Ser
XM_011533072.1:c.284T>G XP_011531374.1:p.Ile95Ser
XM_011533069.2:c.317T>G XP_011531371.1:p.Ile106Ser
XM_011533072.2:c.284T>G XP_011531374.1:p.Ile95Ser
NM_000348.4:c.539T>G MANE Select NP_000339.2:p.Ile180Ser