Canonical Allele Identifier: CA496082717
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67470002G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436099G>C , CM000678.2:g.67436099G>C GRCh38
NC_000016.9:g.67470002G>C , CM000678.1:g.67470002G>C GRCh37
NC_000016.8:g.66027503G>C NCBI36
NG_011482.1:g.50088C>G
NG_016549.1:g.9967G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.621G>C MANE Select ENSP00000316786.5:p.Leu207=
ENST00000326152.5:c.621G>C ENSP00000316786.5:p.Leu207=
ENST00000566606.1:c.599G>C ENSP00000473429.1:n.599G>C
ENST00000567684.2:n.484G>C
NM_000196.3:c.621G>C NP_000187.3:p.Leu207=
NM_000196.4:c.621G>C MANE Select NP_000187.3:p.Leu207=
Search 100 bp 5'
Search 100 bp 3'