Canonical Allele Identifier: CA496082725
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67470008C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436105C>T , CM000678.2:g.67436105C>T GRCh38
NC_000016.9:g.67470008C>T , CM000678.1:g.67470008C>T GRCh37
NC_000016.8:g.66027509C>T NCBI36
NG_011482.1:g.50082G>A
NG_016549.1:g.9973C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.627C>T MANE Select ENSP00000316786.5:p.Ser209=
ENST00000326152.5:c.627C>T ENSP00000316786.5:p.Ser209=
ENST00000566606.1:c.605C>T ENSP00000473429.1:n.605C>T
ENST00000567684.2:n.490C>T
NM_000196.3:c.627C>T NP_000187.3:p.Ser209=
NM_000196.4:c.627C>T MANE Select NP_000187.3:p.Ser209=
Search 100 bp 5'
Search 100 bp 3'