Canonical Allele Identifier: CA346598342
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1160969613
gnomAD v2: 2-31756523-C-G
gnomAD v3: 2-31531453-C-G
gnomAD v4: 2-31531453-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531453C>G , CM000664.2:g.31531453C>G GRCh38
NC_000002.11:g.31756523C>G , CM000664.1:g.31756523C>G GRCh37
NC_000002.10:g.31610027C>G NCBI36
NG_008365.1:g.54519G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.465G>C MANE Select ENSP00000477587.1:p.Leu155Phe
ENST00000622030.1:c.465G>C ENSP00000477587.1:p.Leu155Phe
NM_000348.3:c.465G>C NP_000339.2:p.Leu155Phe
XM_011533069.1:c.243G>C XP_011531371.1:p.Leu81Phe
XM_011533070.1:c.210G>C XP_011531372.1:p.Leu70Phe
XM_011533071.1:c.210G>C XP_011531373.1:p.Leu70Phe
XM_011533072.1:c.210G>C XP_011531374.1:p.Leu70Phe
XM_011533069.2:c.243G>C XP_011531371.1:p.Leu81Phe
XM_011533072.2:c.210G>C XP_011531374.1:p.Leu70Phe
NM_000348.4:c.465G>C MANE Select NP_000339.2:p.Leu155Phe