Canonical Allele Identifier: CA2580060928
Gene: HSD3B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1913134
ClinVar RCV Id: RCV002593642

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119422243_119422247delinsAACT , CM000663.2:g.119422243_119422247delinsAACT GRCh38
NC_000001.10:g.119964866_119964870delinsAACT , CM000663.1:g.119964866_119964870delinsAACT GRCh37
NC_000001.9:g.119766389_119766393delinsAACT NCBI36
NG_013349.1:g.12313_12317delinsAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369416.4:c.742_746delinsAACT MANE Select ENSP00000358424.3:p.Val248AsnfsTer2
ENST00000369416.3:c.742_746delinsAACT ENSP00000358424.3:p.Val248AsnfsTer2
ENST00000543831.5:c.742_746delinsAACT ENSP00000445122.1:p.Val248AsnfsTer2
NM_000198.3:c.742_746delinsAACT NP_000189.1:p.Val248AsnfsTer2
NM_001166120.1:c.742_746delinsAACT NP_001159592.1:p.Val248AsnfsTer2
NM_000198.4:c.742_746delinsAACT MANE Select NP_000189.1:p.Val248AsnfsTer2
NM_001166120.2:c.742_746delinsAACT NP_001159592.1:p.Val248AsnfsTer2