Canonical Allele Identifier: CA396282228
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67470608T>C (hg19) chr16:g.67436705T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436705T>C , CM000678.2:g.67436705T>C GRCh38
NC_000016.9:g.67470608T>C , CM000678.1:g.67470608T>C GRCh37
NC_000016.8:g.66028109T>C NCBI36
NG_011482.1:g.49482A>G
NG_016549.1:g.10573T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.920T>C MANE Select ENSP00000316786.5:p.Phe307Ser
ENST00000326152.5:c.920T>C ENSP00000316786.5:p.Phe307Ser
NM_000196.3:c.920T>C NP_000187.3:p.Phe307Ser
NM_000196.4:c.920T>C MANE Select NP_000187.3:p.Phe307Ser
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Search 100 bp 3'