Canonical Allele Identifier: CA1192292868
Gene: HSD3B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119422242_119422245delinsTGTC , CM000663.2:g.119422242_119422245delinsTGTC GRCh38
NC_000001.10:g.119964865_119964868delinsTGTC , CM000663.1:g.119964865_119964868delinsTGTC GRCh37
NC_000001.9:g.119766388_119766391delinsTGTC NCBI36
NG_013349.1:g.12312_12315delinsTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369416.4:c.741_744delinsTGTC MANE Select ENSP00000358424.3:p.Ser247=
ENST00000369416.3:c.741_744delinsTGTC ENSP00000358424.3:p.Ser247=
ENST00000543831.5:c.741_744delinsTGTC ENSP00000445122.1:p.Ser247=
NM_000198.3:c.741_744delinsTGTC NP_000189.1:p.Ser247=
NM_001166120.1:c.741_744delinsTGTC NP_001159592.1:p.Ser247=
NM_000198.4:c.741_744delinsTGTC MANE Select NP_000189.1:p.Ser247=
NM_001166120.2:c.741_744delinsTGTC NP_001159592.1:p.Ser247=