Canonical Allele Identifier: CA11182305
Gene: SRD5A2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs676033

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31583901T>C , CM000664.2:g.31583901T>C GRCh38
NC_000002.11:g.31808970T>C , CM000664.1:g.31808970T>C GRCh37
NC_000002.10:g.31662474T>C NCBI36
NG_008365.1:g.2071A>G

Transcript Alleles

HGVS Amino-acid change
XM_011533070.1:c.27-50135A>G XP_011531372.1:p.=
XM_011533071.1:c.27-50135A>G XP_011531373.1:p.=
XM_011533072.1:c.27-50135A>G XP_011531374.1:p.=
XM_011533072.2:c.27-50135A>G XP_011531374.1:p.=