Canonical Allele Identifier: CA767792667
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1299935825
gnomAD v3: 2-31586706-A-C
gnomAD v4: 2-31586706-A-C
MyVariant Identifiers: chr2:g.31811775A>C (hg19) chr2:g.31586706A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31586706A>C , CM000664.2:g.31586706A>C GRCh38
NC_000002.11:g.31811775A>C , CM000664.1:g.31811775A>C GRCh37
NC_000002.10:g.31665279A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011533070.1:c.27-52940T>G XP_011531372.1:n.27-52940T>G
XM_011533071.1:c.27-52940T>G XP_011531373.1:n.27-52940T>G
XM_011533072.1:c.27-52940T>G XP_011531374.1:n.27-52940T>G
XM_011533072.2:c.27-52940T>G XP_011531374.1:n.27-52940T>G
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