Canonical Allele Identifier: CA463327008

Gene: CYP11B1 GML

Linked Data

• dbSNP Id: rs1816926228
• gnomAD v4: 8-142875834-G-A
• MyVariant Identifiers: chr8:g.143957250G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875834G>A , CM000670.2:g.142875834G>A	GRCh38
NC_000008.10:g.143957250G>A , CM000670.1:g.143957250G>A	GRCh37
NC_000008.9:g.143954252G>A	NCBI36
NG_007954.1:g.8987C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.999C>T (CYP11B1) MANE Select	ENSP00000292427.5:p.Asn333=
ENST00000292427.8:c.999C>T (CYP11B1)	ENSP00000292427.4:p.Asn333=
ENST00000314111.4:n.1394C>T (CYP11B1)
ENST00000377675.3:c.1212C>T (CYP11B1)	ENSP00000366903.3:p.Asn404=
ENST00000517471.5:c.999C>T (CYP11B1)	ENSP00000428043.1:p.Asn333=
ENST00000522728.5:c.181+34609G>A (GML)	ENSP00000430799.1:n.181+34609G>A
NM_000497.3:c.999C>T (CYP11B1)	NP_000488.3:p.Asn333=
NM_001026213.1:c.999C>T (CYP11B1)	NP_001021384.1:p.Asn333=
XM_011516870.1:c.1077C>T (CYP11B1)	XP_011515172.1:p.Asn359=
XM_011516871.1:c.1077C>T (CYP11B1)	XP_011515173.1:p.Asn359=
XM_011516872.1:c.999C>T (CYP11B1)	XP_011515174.1:p.Asn333=
XM_011516873.1:c.1077C>T (CYP11B1)	XP_011515175.1:p.Asn359=
XM_011516874.1:c.1077C>T (CYP11B1)	XP_011515176.1:p.Asn359=
XM_011516875.1:c.816C>T (CYP11B1)	XP_011515177.1:p.Asn272=
XM_011516876.1:c.1077C>T (CYP11B1)	XP_011515178.1:p.Asn359=
XM_011516970.1:c.214+34609G>A (GML)	XP_011515272.1:n.214+34609G>A
NM_000497.4:c.999C>T (CYP11B1) MANE Select	NP_000488.3:p.Asn333=