Canonical Allele Identifier: CA282322790
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs929639516
MyVariant Identifiers: chr16:g.67470125G>A (hg19) chr16:g.67436222G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436222G>A , CM000678.2:g.67436222G>A GRCh38
NC_000016.9:g.67470125G>A , CM000678.1:g.67470125G>A GRCh37
NC_000016.8:g.66027626G>A NCBI36
NG_011482.1:g.49965C>T
NG_016549.1:g.10090G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.665-27G>A MANE Select ENSP00000316786.5:n.665-27G>A
ENST00000326152.5:c.665-27G>A ENSP00000316786.5:n.665-27G>A
ENST00000567684.2:n.528-27G>A
NM_000196.3:c.665-27G>A NP_000187.3:n.665-27G>A
NM_000196.4:c.665-27G>A MANE Select NP_000187.3:n.665-27G>A
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