Canonical Allele Identifier: CA346598176
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531380T>G , CM000664.2:g.31531380T>G GRCh38
NC_000002.11:g.31756450T>G , CM000664.1:g.31756450T>G GRCh37
NC_000002.10:g.31609954T>G NCBI36
NG_008365.1:g.54592A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.538A>C MANE Select ENSP00000477587.1:p.Ile180Leu
ENST00000622030.1:c.538A>C ENSP00000477587.1:p.Ile180Leu
NM_000348.3:c.538A>C NP_000339.2:p.Ile180Leu
XM_011533069.1:c.316A>C XP_011531371.1:p.Ile106Leu
XM_011533070.1:c.283A>C XP_011531372.1:p.Ile95Leu
XM_011533071.1:c.283A>C XP_011531373.1:p.Ile95Leu
XM_011533072.1:c.283A>C XP_011531374.1:p.Ile95Leu
XM_011533069.2:c.316A>C XP_011531371.1:p.Ile106Leu
XM_011533072.2:c.283A>C XP_011531374.1:p.Ile95Leu
NM_000348.4:c.538A>C MANE Select NP_000339.2:p.Ile180Leu