Canonical Allele Identifier: CA2807429688

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436156_67436157insAAA , CM000678.2:g.67436156_67436157insAAA	GRCh38
NC_000016.9:g.67470059_67470060insAAA , CM000678.1:g.67470059_67470060insAAA	GRCh37
NC_000016.8:g.66027560_66027561insAAA	NCBI36
NG_011482.1:g.50030_50031insTTT
NG_016549.1:g.10024_10025insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.664+14_664+15insAAA MANE Select	ENSP00000316786.5:n.664+14_664+15insAAA
ENST00000326152.5:c.664+14_664+15insAAA	ENSP00000316786.5:n.664+14_664+15insAAA
ENST00000567684.2:n.527+14_527+15insAAA
NM_000196.3:c.664+14_664+15insAAA	NP_000187.3:n.664+14_664+15insAAA
NM_000196.4:c.664+14_664+15insAAA MANE Select	NP_000187.3:n.664+14_664+15insAAA