Canonical Allele Identifier: CA767790888
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1177035254
gnomAD v3: 2-31583827-A-G
gnomAD v4: 2-31583827-A-G
MyVariant Identifiers: chr2:g.31808896A>G (hg19) chr2:g.31583827A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31583827A>G , CM000664.2:g.31583827A>G GRCh38
NC_000002.11:g.31808896A>G , CM000664.1:g.31808896A>G GRCh37
NC_000002.10:g.31662400A>G NCBI36
NG_008365.1:g.2145T>C

Transcript Alleles

HGVS Amino-acid change
XM_011533070.1:c.27-50061T>C XP_011531372.1:n.27-50061T>C
XM_011533071.1:c.27-50061T>C XP_011531373.1:n.27-50061T>C
XM_011533072.1:c.27-50061T>C XP_011531374.1:n.27-50061T>C
XM_011533072.2:c.27-50061T>C XP_011531374.1:n.27-50061T>C
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