Canonical Allele Identifier: CA767779469
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1196834327
MyVariant Identifiers: chr2:g.31792649del (hg19) chr2:g.31567579del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31567580del , CM000664.2:g.31567580del GRCh38
NC_000002.11:g.31792650del , CM000664.1:g.31792650del GRCh37
NC_000002.10:g.31646154del NCBI36
NG_008365.1:g.18393del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+13041del MANE Select ENSP00000477587.1:n.281+13041del
ENST00000622030.1:c.281+13041del ENSP00000477587.1:n.281+13041del
NM_000348.3:c.281+13041del NP_000339.2:n.281+13041del
XM_011533068.1:c.281+13041del XP_011531370.1:n.281+13041del
XM_011533070.1:c.27-33813del XP_011531372.1:n.27-33813del
XM_011533071.1:c.27-33813del XP_011531373.1:n.27-33813del
XM_011533072.1:c.27-33813del XP_011531374.1:n.27-33813del
XM_011533072.2:c.27-33813del XP_011531374.1:n.27-33813del
NM_000348.4:c.281+13041del MANE Select NP_000339.2:n.281+13041del
Search 100 bp 5'
Search 100 bp 3'