Canonical Allele Identifier: CA1028969095
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1405447161
gnomAD v3: 2-31567504-T-C
gnomAD v4: 2-31567504-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31567504T>C , CM000664.2:g.31567504T>C GRCh38
NC_000002.11:g.31792574T>C , CM000664.1:g.31792574T>C GRCh37
NC_000002.10:g.31646078T>C NCBI36
NG_008365.1:g.18468A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+13116A>G MANE Select ENSP00000477587.1:n.281+13116A>G
ENST00000622030.1:c.281+13116A>G ENSP00000477587.1:n.281+13116A>G
NM_000348.3:c.281+13116A>G NP_000339.2:n.281+13116A>G
XM_011533068.1:c.281+13116A>G XP_011531370.1:n.281+13116A>G
XM_011533070.1:c.27-33738A>G XP_011531372.1:n.27-33738A>G
XM_011533071.1:c.27-33738A>G XP_011531373.1:n.27-33738A>G
XM_011533072.1:c.27-33738A>G XP_011531374.1:n.27-33738A>G
XM_011533072.2:c.27-33738A>G XP_011531374.1:n.27-33738A>G
NM_000348.4:c.281+13116A>G MANE Select NP_000339.2:n.281+13116A>G
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