Canonical Allele Identifier: CA767792670
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1288020370
gnomAD v3: 2-31586712-T-C
gnomAD v4: 2-31586712-T-C
MyVariant Identifiers: chr2:g.31811781T>C (hg19) chr2:g.31586712T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31586712T>C , CM000664.2:g.31586712T>C GRCh38
NC_000002.11:g.31811781T>C , CM000664.1:g.31811781T>C GRCh37
NC_000002.10:g.31665285T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011533070.1:c.27-52946A>G XP_011531372.1:n.27-52946A>G
XM_011533071.1:c.27-52946A>G XP_011531373.1:n.27-52946A>G
XM_011533072.1:c.27-52946A>G XP_011531374.1:n.27-52946A>G
XM_011533072.2:c.27-52946A>G XP_011531374.1:n.27-52946A>G
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