Canonical Allele Identifier: CA396279587
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67470007G>T (hg19) chr16:g.67436104G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436104G>T , CM000678.2:g.67436104G>T GRCh38
NC_000016.9:g.67470007G>T , CM000678.1:g.67470007G>T GRCh37
NC_000016.8:g.66027508G>T NCBI36
NG_011482.1:g.50083C>A
NG_016549.1:g.9972G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.626G>T MANE Select ENSP00000316786.5:p.Ser209Ile
ENST00000326152.5:c.626G>T ENSP00000316786.5:p.Ser209Ile
ENST00000566606.1:c.604G>T ENSP00000473429.1:n.604G>T
ENST00000567684.2:n.489G>T
NM_000196.3:c.626G>T NP_000187.3:p.Ser209Ile
NM_000196.4:c.626G>T MANE Select NP_000187.3:p.Ser209Ile
Search 100 bp 5'
Search 100 bp 3'