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ClinGen Allele Registry
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Canonical Allele Identifier:
CA2229309718
Community Standard Title: NM_000196.4(HSD11B2):c.623G= (p.Arg208=)
Gene: HSD11B2
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.67436101G= , CM000678.2:g.67436101G=
GRCh38
NC_000016.9:g.67470004G= , CM000678.1:g.67470004G=
GRCh37
NC_000016.8:g.66027505G=
NCBI36
NG_011482.1:g.50086C=
NG_016549.1:g.9969G=
Transcript Alleles
HGVS
Amino-acid Change
NM_000196.4:c.623G=
MANE Select
NP_000187.3:p.Arg208=
ENST00000326152.6:c.623G=
MANE Select
ENSP00000316786.5:p.Arg208=
NM_000196.3:c.623G=
NP_000187.3:p.Arg208=
ENST00000326152.5:c.623G=
ENSP00000316786.5:p.Arg208=
ENST00000566606.1:c.601G=
ENSP00000473429.1:n.601G=
ENST00000567684.2:n.486G=
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