Canonical Allele Identifier: CA2807429771
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436450dup , CM000678.2:g.67436450dup GRCh38
NC_000016.9:g.67470353dup , CM000678.1:g.67470353dup GRCh37
NC_000016.8:g.66027854dup NCBI36
NG_011482.1:g.49741dup
NG_016549.1:g.10318dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.802+64dup MANE Select ENSP00000316786.5:n.802+64dup
ENST00000326152.5:c.802+64dup ENSP00000316786.5:n.802+64dup
NM_000196.3:c.802+64dup NP_000187.3:n.802+64dup
NM_000196.4:c.802+64dup MANE Select NP_000187.3:n.802+64dup
Search 100 bp 5'
Search 100 bp 3'