Canonical Allele Identifier: CA2807429703

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436171_67436172insAACCAAACACACCCAACACA , CM000678.2:g.67436171_67436172insAACCAAACACACCCAACACA	GRCh38
NC_000016.9:g.67470074_67470075insAACCAAACACACCCAACACA , CM000678.1:g.67470074_67470075insAACCAAACACACCCAACACA	GRCh37
NC_000016.8:g.66027575_66027576insAACCAAACACACCCAACACA	NCBI36
NG_011482.1:g.50016_50017insGTGTTGGGTGTGTTTGGTTT
NG_016549.1:g.10039_10040insAACCAAACACACCCAACACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.664+29_664+30insAACCAAACACACCCAACACA MANE Select	ENSP00000316786.5:n.664+29_664+30insAACCAAACACACCCAACACA
ENST00000326152.5:c.664+29_664+30insAACCAAACACACCCAACACA	ENSP00000316786.5:n.664+29_664+30insAACCAAACACACCCAACACA
ENST00000567684.2:n.527+29_527+30insAACCAAACACACCCAACACA
NM_000196.3:c.664+29_664+30insAACCAAACACACCCAACACA	NP_000187.3:n.664+29_664+30insAACCAAACACACCCAACACA
NM_000196.4:c.664+29_664+30insAACCAAACACACCCAACACA MANE Select	NP_000187.3:n.664+29_664+30insAACCAAACACACCCAACACA