Canonical Allele Identifier: CA767792852
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1323435798
gnomAD v3: 2-31586843-A-G
gnomAD v4: 2-31586843-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31586843A>G , CM000664.2:g.31586843A>G GRCh38
NC_000002.11:g.31811912A>G , CM000664.1:g.31811912A>G GRCh37
NC_000002.10:g.31665416A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011533070.1:c.27-53077T>C XP_011531372.1:n.27-53077T>C
XM_011533071.1:c.27-53077T>C XP_011531373.1:n.27-53077T>C
XM_011533072.1:c.27-53077T>C XP_011531374.1:n.27-53077T>C
XM_011533072.2:c.27-53077T>C XP_011531374.1:n.27-53077T>C