Canonical Allele Identifier: CA2576029231
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436696_67436697insCTACAT , CM000678.2:g.67436696_67436697insCTACAT GRCh38
NC_000016.9:g.67470599_67470600insCTACAT , CM000678.1:g.67470599_67470600insCTACAT GRCh37
NC_000016.8:g.66028100_66028101insCTACAT NCBI36
NG_011482.1:g.49490_49491insATGTAG
NG_016549.1:g.10564_10565insCTACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.911_912insCTACAT MANE Select ENSP00000316786.5:p.His304_Gly305insTyrIle
ENST00000326152.5:c.911_912insCTACAT ENSP00000316786.5:p.His304_Gly305insTyrIle
NM_000196.3:c.911_912insCTACAT NP_000187.3:p.His304_Gly305insTyrIle
NM_000196.4:c.911_912insCTACAT MANE Select NP_000187.3:p.His304_Gly305insTyrIle
Search 100 bp 5'
Search 100 bp 3'