Canonical Allele Identifier: CA2229309567
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435988_67435989delinsCA , CM000678.2:g.67435988_67435989delinsCA GRCh38
NC_000016.9:g.67469891_67469892delinsCA , CM000678.1:g.67469891_67469892delinsCA GRCh37
NC_000016.8:g.66027392_66027393delinsCA NCBI36
NG_016549.1:g.9856_9857delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.510_511delinsCA MANE Select ENSP00000316786.5:p.His170=
ENST00000326152.5:c.510_511delinsCA ENSP00000316786.5:p.His170=
ENST00000566606.1:c.488_489delinsCA ENSP00000473429.1:n.488_489delinsCA
ENST00000567684.2:n.373_374delinsCA
NM_000196.3:c.510_511delinsCA NP_000187.3:p.His170=
NM_000196.4:c.510_511delinsCA MANE Select NP_000187.3:p.His170=
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Search 100 bp 3'