Canonical Allele Identifier: CA282323082
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs760848811
gnomAD v4: 16-67436536-G-C
MyVariant Identifiers: chr16:g.67470439G>C (hg19) chr16:g.67436536G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436536G>C , CM000678.2:g.67436536G>C GRCh38
NC_000016.9:g.67470439G>C , CM000678.1:g.67470439G>C GRCh37
NC_000016.8:g.66027940G>C NCBI36
NG_011482.1:g.49651C>G
NG_016549.1:g.10404G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.803-52G>C MANE Select ENSP00000316786.5:n.803-52G>C
ENST00000326152.5:c.803-52G>C ENSP00000316786.5:n.803-52G>C
NM_000196.3:c.803-52G>C NP_000187.3:n.803-52G>C
NM_000196.4:c.803-52G>C MANE Select NP_000187.3:n.803-52G>C
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