Canonical Allele Identifier: CA623119773
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs1304261961
gnomAD v2: 16-67470934-G-A
gnomAD v4: 16-67437031-G-A
MyVariant Identifiers: chr16:g.67470934G>A (hg19) chr16:g.67437031G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437031G>A , CM000678.2:g.67437031G>A GRCh38
NC_000016.9:g.67470934G>A , CM000678.1:g.67470934G>A GRCh37
NC_000016.8:g.66028435G>A NCBI36
NG_011482.1:g.49156C>T
NG_016549.1:g.10899G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*28G>A MANE Select ENSP00000316786.5:n.*28G>A
ENST00000326152.5:c.*28G>A ENSP00000316786.5:n.*28G>A
NM_000196.3:c.*28G>A NP_000187.3:n.*28G>A
NM_000196.4:c.*28G>A MANE Select NP_000187.3:n.*28G>A
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