Canonical Allele Identifier: CA8110850
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs72650126
ExAC: 16:67470946 G / A
gnomAD v2: 16-67470946-G-A
gnomAD v3: 16-67437043-G-A
gnomAD v4: 16-67437043-G-A
MyVariant Identifiers: chr16:g.67470946G>A (hg19) chr16:g.67437043G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437043G>A , CM000678.2:g.67437043G>A GRCh38
NC_000016.9:g.67470946G>A , CM000678.1:g.67470946G>A GRCh37
NC_000016.8:g.66028447G>A NCBI36
NG_011482.1:g.49144C>T
NG_016549.1:g.10911G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*40G>A MANE Select ENSP00000316786.5:n.*40G>A
ENST00000326152.5:c.*40G>A ENSP00000316786.5:n.*40G>A
NM_000196.3:c.*40G>A NP_000187.3:n.*40G>A
NM_000196.4:c.*40G>A MANE Select NP_000187.3:n.*40G>A
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