Canonical Allele Identifier: CA767785335
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1355284497

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31612309_31612312del , CM000664.2:g.31612309_31612312del GRCh38
NC_000002.11:g.31837378_31837381del , CM000664.1:g.31837378_31837381del GRCh37
NC_000002.10:g.31690882_31690885del NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011533070.1:c.26+34011_26+34014del XP_011531372.1:n.26+34011_26+34014del
XM_011533071.1:c.26+34011_26+34014del XP_011531373.1:n.26+34011_26+34014del
XM_011533072.1:c.26+34011_26+34014del XP_011531374.1:n.26+34011_26+34014del
XM_011533072.2:c.26+34011_26+34014del XP_011531374.1:n.26+34011_26+34014del