Canonical Allele Identifier: CA2688875633
Gene: CYP11B2 HGNC NCBI
GML HGNC NCBI

Linked Data

gnomAD v4: 8-142911850-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142911850A>G , CM000670.2:g.142911850A>G GRCh38
NC_000008.10:g.143993266A>G , CM000670.1:g.143993266A>G GRCh37
NC_000008.9:g.143990268A>G NCBI36
NG_008374.1:g.10994T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.*130T>C (CYP11B2) MANE Select ENSP00000325822.2:n.*130T>C
ENST00000522728.5:c.182-2113A>G (GML) ENSP00000430799.1:n.182-2113A>G
NM_000498.3:c.*130T>C (CYP11B2) MANE Select NP_000489.3:n.*130T>C
XM_011516877.1:c.*130T>C (CYP11B2) XP_011515179.1:n.*130T>C
XM_011516878.1:c.*130T>C (CYP11B2) XP_011515180.1:n.*130T>C
XM_011516879.1:c.*130T>C (CYP11B2) XP_011515181.1:n.*130T>C
XM_011516970.1:c.215-2113A>G (GML) XP_011515272.1:n.215-2113A>G
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