Canonical Allele Identifier: CA8110845
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs767212765
ExAC: 16:67470915 C / T
gnomAD v2: 16-67470915-C-T
gnomAD v4: 16-67437012-C-T
MyVariant Identifiers: chr16:g.67470915C>T (hg19) chr16:g.67437012C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437012C>T , CM000678.2:g.67437012C>T GRCh38
NC_000016.9:g.67470915C>T , CM000678.1:g.67470915C>T GRCh37
NC_000016.8:g.66028416C>T NCBI36
NG_011482.1:g.49175G>A
NG_016549.1:g.10880C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*9C>T MANE Select ENSP00000316786.5:n.*9C>T
ENST00000326152.5:c.*9C>T ENSP00000316786.5:n.*9C>T
NM_000196.3:c.*9C>T NP_000187.3:n.*9C>T
NM_000196.4:c.*9C>T MANE Select NP_000187.3:n.*9C>T
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