Canonical Allele Identifier: CA11006418
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs612224
gnomAD v2: 2-31811870-C-A
gnomAD v3: 2-31586801-C-A
gnomAD v4: 2-31586801-C-A
MyVariant Identifiers: chr2:g.31811870C>A (hg19) chr2:g.31586801C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31586801C>A , CM000664.2:g.31586801C>A GRCh38
NC_000002.11:g.31811870C>A , CM000664.1:g.31811870C>A GRCh37
NC_000002.10:g.31665374C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011533070.1:c.27-53035G>T XP_011531372.1:n.27-53035G>T
XM_011533071.1:c.27-53035G>T XP_011531373.1:n.27-53035G>T
XM_011533072.1:c.27-53035G>T XP_011531374.1:n.27-53035G>T
XM_011533072.2:c.27-53035G>T XP_011531374.1:n.27-53035G>T
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