Canonical Allele Identifier: CA396279071
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67469925G>A (hg19) chr16:g.67436022G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436022G>A , CM000678.2:g.67436022G>A GRCh38
NC_000016.9:g.67469925G>A , CM000678.1:g.67469925G>A GRCh37
NC_000016.8:g.66027426G>A NCBI36
NG_011482.1:g.50165C>T
NG_016549.1:g.9890G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.544G>A MANE Select ENSP00000316786.5:p.Val182Met
ENST00000326152.5:c.544G>A ENSP00000316786.5:p.Val182Met
ENST00000566606.1:c.522G>A ENSP00000473429.1:n.522G>A
ENST00000567684.2:n.407G>A
NM_000196.3:c.544G>A NP_000187.3:p.Val182Met
NM_000196.4:c.544G>A MANE Select NP_000187.3:p.Val182Met
Search 100 bp 5'
Search 100 bp 3'