Canonical Allele Identifier: CA2229310189
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436424A= , CM000678.2:g.67436424A= GRCh38
NC_000016.9:g.67470327A= , CM000678.1:g.67470327A= GRCh37
NC_000016.8:g.66027828A= NCBI36
NG_011482.1:g.49763T=
NG_016549.1:g.10292A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.802+38A= MANE Select ENSP00000316786.5:n.802+38A=
ENST00000326152.5:c.802+38A= ENSP00000316786.5:n.802+38A=
NM_000196.3:c.802+38A= NP_000187.3:n.802+38A=
NM_000196.4:c.802+38A= MANE Select NP_000187.3:n.802+38A=
Search 100 bp 5'
Search 100 bp 3'