Canonical Allele Identifier: CA396278851
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67469883G>C (hg19) chr16:g.67435980G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435980G>C , CM000678.2:g.67435980G>C GRCh38
NC_000016.9:g.67469883G>C , CM000678.1:g.67469883G>C GRCh37
NC_000016.8:g.66027384G>C NCBI36
NG_016549.1:g.9848G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.502G>C MANE Select ENSP00000316786.5:p.Ala168Pro
ENST00000326152.5:c.502G>C ENSP00000316786.5:p.Ala168Pro
ENST00000566606.1:c.480G>C ENSP00000473429.1:n.480G>C
ENST00000567684.2:n.365G>C
NM_000196.3:c.502G>C NP_000187.3:p.Ala168Pro
NM_000196.4:c.502G>C MANE Select NP_000187.3:p.Ala168Pro
Search 100 bp 5'
Search 100 bp 3'