Canonical Allele Identifier: CA372392143

Gene: CYP11B1 GML

Linked Data

• gnomAD v4: 8-142875235-C-A
• MyVariant Identifiers: chr8:g.143956651C>A (hg19) ; chr8:g.142875235C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875235C>A , CM000670.2:g.142875235C>A	GRCh38
NC_000008.10:g.143956651C>A , CM000670.1:g.143956651C>A	GRCh37
NC_000008.9:g.143953653C>A	NCBI36
NG_007954.1:g.9586G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1199G>T (CYP11B1) MANE Select	ENSP00000292427.5:p.Gly400Val
ENST00000292427.8:c.1199G>T (CYP11B1)	ENSP00000292427.4:p.Gly400Val
ENST00000314111.4:n.1594G>T (CYP11B1)
ENST00000377675.3:c.1412G>T (CYP11B1)	ENSP00000366903.3:p.Gly471Val
ENST00000517471.5:c.1199G>T (CYP11B1)	ENSP00000428043.1:p.Gly400Val
ENST00000519285.5:c.233G>T (CYP11B1)	ENSP00000430144.1:p.Gly78Val
ENST00000522728.5:c.181+34010C>A (GML)	ENSP00000430799.1:n.181+34010C>A
NM_000497.3:c.1199G>T (CYP11B1)	NP_000488.3:p.Gly400Val
NM_001026213.1:c.1199G>T (CYP11B1)	NP_001021384.1:p.Gly400Val
XM_011516870.1:c.1346G>T (CYP11B1)	XP_011515172.1:p.Gly449Val
XM_011516871.1:c.1277G>T (CYP11B1)	XP_011515173.1:p.Gly426Val
XM_011516872.1:c.1268G>T (CYP11B1)	XP_011515174.1:p.Gly423Val
XM_011516873.1:c.1346G>T (CYP11B1)	XP_011515175.1:p.Gly449Val
XM_011516874.1:c.1277G>T (CYP11B1)	XP_011515176.1:p.Gly426Val
XM_011516875.1:c.1085G>T (CYP11B1)	XP_011515177.1:p.Gly362Val
XM_011516876.1:c.1346G>T (CYP11B1)	XP_011515178.1:p.Gly449Val
XM_011516970.1:c.214+34010C>A (GML)	XP_011515272.1:n.214+34010C>A
NM_000497.4:c.1199G>T (CYP11B1) MANE Select	NP_000488.3:p.Gly400Val