Canonical Allele Identifier: CA767790883
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1177035254

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31583827A>C , CM000664.2:g.31583827A>C GRCh38
NC_000002.11:g.31808896A>C , CM000664.1:g.31808896A>C GRCh37
NC_000002.10:g.31662400A>C NCBI36
NG_008365.1:g.2145T>G

Transcript Alleles

HGVS Amino-acid change
XM_011533070.1:c.27-50061T>G XP_011531372.1:n.27-50061T>G
XM_011533071.1:c.27-50061T>G XP_011531373.1:n.27-50061T>G
XM_011533072.1:c.27-50061T>G XP_011531374.1:n.27-50061T>G
XM_011533072.2:c.27-50061T>G XP_011531374.1:n.27-50061T>G