Canonical Allele Identifier: CA1192293693
Gene: HSD3B2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119422877C= , CM000663.2:g.119422877C= GRCh38
NC_000001.10:g.119965500C= , CM000663.1:g.119965500C= GRCh37
NC_000001.9:g.119767023C= NCBI36
NG_013349.1:g.12947C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369416.4:c.*257C= MANE Select ENSP00000358424.3:n.*257C=
ENST00000369416.3:c.*257C= ENSP00000358424.3:n.*257C=
ENST00000543831.5:c.*257C= ENSP00000445122.1:n.*257C=
NM_000198.3:c.*257C= NP_000189.1:n.*257C=
NM_001166120.1:c.*257C= NP_001159592.1:n.*257C=
NM_000198.4:c.*257C= MANE Select NP_000189.1:n.*257C=
NM_001166120.2:c.*257C= NP_001159592.1:n.*257C=
Search 100 bp 5'
Search 100 bp 3'