Canonical Allele Identifier: CA2807429691

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436157_67436158insAACAACCAAACACACCCAACA , CM000678.2:g.67436157_67436158insAACAACCAAACACACCCAACA	GRCh38
NC_000016.9:g.67470060_67470061insAACAACCAAACACACCCAACA , CM000678.1:g.67470060_67470061insAACAACCAAACACACCCAACA	GRCh37
NC_000016.8:g.66027561_66027562insAACAACCAAACACACCCAACA	NCBI36
NG_011482.1:g.50029_50030insTGTTGGGTGTGTTTGGTTGTT
NG_016549.1:g.10025_10026insAACAACCAAACACACCCAACA

Transcript Alleles

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