Canonical Allele Identifier: CA767792844
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1205915795
gnomAD v3: 2-31586828-C-T
gnomAD v4: 2-31586828-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31586828C>T , CM000664.2:g.31586828C>T GRCh38
NC_000002.11:g.31811897C>T , CM000664.1:g.31811897C>T GRCh37
NC_000002.10:g.31665401C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011533070.1:c.27-53062G>A XP_011531372.1:n.27-53062G>A
XM_011533071.1:c.27-53062G>A XP_011531373.1:n.27-53062G>A
XM_011533072.1:c.27-53062G>A XP_011531374.1:n.27-53062G>A
XM_011533072.2:c.27-53062G>A XP_011531374.1:n.27-53062G>A