Canonical Allele Identifier: CA4906097
Gene: CYP11B2 HGNC NCBI
GML HGNC NCBI

Linked Data

ClinVar Variation Id: 793072
ClinVar RCV Id: RCV000976227 RCV001271155
dbSNP Id: rs748615718
ExAC: 8:143996152 G / A
gnomAD v4: 8-142914736-G-A
MyVariant Identifiers: chr8:g.143996152G>A (hg19) chr8:g.142914736G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914736G>A , CM000670.2:g.142914736G>A GRCh38
NC_000008.10:g.143996152G>A , CM000670.1:g.143996152G>A GRCh37
NC_000008.9:g.143993154G>A NCBI36
NG_008374.1:g.8108C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.768C>T (CYP11B2) MANE Select ENSP00000325822.2:p.His256=
ENST00000522728.5:c.264+691G>A (GML) ENSP00000430799.1:n.264+691G>A
NM_000498.3:c.768C>T (CYP11B2) MANE Select NP_000489.3:p.His256=
XM_011516877.1:c.846C>T (CYP11B2) XP_011515179.1:p.His282=
XM_011516878.1:c.846C>T (CYP11B2) XP_011515180.1:p.His282=
XM_011516879.1:c.768C>T (CYP11B2) XP_011515181.1:p.His256=
XM_011516970.1:c.297+691G>A (GML) XP_011515272.1:n.297+691G>A
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