Canonical Allele Identifier: CA2633778734
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67435562-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435562T>G , CM000678.2:g.67435562T>G GRCh38
NC_000016.9:g.67469465T>G , CM000678.1:g.67469465T>G GRCh37
NC_000016.8:g.66026966T>G NCBI36
NG_016549.1:g.9430T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.266-66T>G MANE Select ENSP00000316786.5:n.266-66T>G
ENST00000326152.5:c.266-66T>G ENSP00000316786.5:n.266-66T>G
ENST00000566606.1:c.178T>G ENSP00000473429.1:n.178T>G
ENST00000567684.2:n.129-66T>G
NM_000196.3:c.266-66T>G NP_000187.3:n.266-66T>G
NM_000196.4:c.266-66T>G MANE Select NP_000187.3:n.266-66T>G
Search 100 bp 5'
Search 100 bp 3'