Canonical Allele Identifier: CA767779061
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1268568432
MyVariant Identifiers: chr2:g.31792288T>G (hg19) chr2:g.31567218T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31567218T>G , CM000664.2:g.31567218T>G GRCh38
NC_000002.11:g.31792288T>G , CM000664.1:g.31792288T>G GRCh37
NC_000002.10:g.31645792T>G NCBI36
NG_008365.1:g.18754A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+13402A>C MANE Select ENSP00000477587.1:n.281+13402A>C
ENST00000622030.1:c.281+13402A>C ENSP00000477587.1:n.281+13402A>C
NM_000348.3:c.281+13402A>C NP_000339.2:n.281+13402A>C
XM_011533068.1:c.281+13402A>C XP_011531370.1:n.281+13402A>C
XM_011533070.1:c.27-33452A>C XP_011531372.1:n.27-33452A>C
XM_011533071.1:c.27-33452A>C XP_011531373.1:n.27-33452A>C
XM_011533072.1:c.27-33452A>C XP_011531374.1:n.27-33452A>C
XM_011533072.2:c.27-33452A>C XP_011531374.1:n.27-33452A>C
NM_000348.4:c.281+13402A>C MANE Select NP_000339.2:n.281+13402A>C
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