Canonical Allele Identifier: CA767785332
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1375963180

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31612303G>C , CM000664.2:g.31612303G>C GRCh38
NC_000002.11:g.31837372G>C , CM000664.1:g.31837372G>C GRCh37
NC_000002.10:g.31690876G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011533070.1:c.26+34015C>G XP_011531372.1:n.26+34015C>G
XM_011533071.1:c.26+34015C>G XP_011531373.1:n.26+34015C>G
XM_011533072.1:c.26+34015C>G XP_011531374.1:n.26+34015C>G
XM_011533072.2:c.26+34015C>G XP_011531374.1:n.26+34015C>G