Canonical Allele Identifier: CA2807429692

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436157_67436158insACACCCAACA , CM000678.2:g.67436157_67436158insACACCCAACA	GRCh38
NC_000016.9:g.67470060_67470061insACACCCAACA , CM000678.1:g.67470060_67470061insACACCCAACA	GRCh37
NC_000016.8:g.66027561_66027562insACACCCAACA	NCBI36
NG_011482.1:g.50029_50030insTGTTGGGTGT
NG_016549.1:g.10025_10026insACACCCAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.664+15_664+16insACACCCAACA MANE Select	ENSP00000316786.5:n.664+15_664+16insACACCCAACA
ENST00000326152.5:c.664+15_664+16insACACCCAACA	ENSP00000316786.5:n.664+15_664+16insACACCCAACA
ENST00000567684.2:n.527+15_527+16insACACCCAACA
NM_000196.3:c.664+15_664+16insACACCCAACA	NP_000187.3:n.664+15_664+16insACACCCAACA
NM_000196.4:c.664+15_664+16insACACCCAACA MANE Select	NP_000187.3:n.664+15_664+16insACACCCAACA