Canonical Allele Identifier: CA1599926
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs768525253
gnomAD v2: 2-31756515-C-T
gnomAD v4: 2-31531445-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531445C>T , CM000664.2:g.31531445C>T GRCh38
NC_000002.11:g.31756515C>T , CM000664.1:g.31756515C>T GRCh37
NC_000002.10:g.31610019C>T NCBI36
NG_008365.1:g.54527G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.473G>A MANE Select ENSP00000477587.1:p.Gly158Glu
ENST00000622030.1:c.473G>A ENSP00000477587.1:p.Gly158Glu
NM_000348.3:c.473G>A NP_000339.2:p.Gly158Glu
XM_011533069.1:c.251G>A XP_011531371.1:p.Gly84Glu
XM_011533070.1:c.218G>A XP_011531372.1:p.Gly73Glu
XM_011533071.1:c.218G>A XP_011531373.1:p.Gly73Glu
XM_011533072.1:c.218G>A XP_011531374.1:p.Gly73Glu
XM_011533069.2:c.251G>A XP_011531371.1:p.Gly84Glu
XM_011533072.2:c.218G>A XP_011531374.1:p.Gly73Glu
NM_000348.4:c.473G>A MANE Select NP_000339.2:p.Gly158Glu