Canonical Allele Identifier: CA463325045

Gene: CYP11B1 GML

Linked Data

• MyVariant Identifiers: chr8:g.143955843G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142874427G>A , CM000670.2:g.142874427G>A	GRCh38
NC_000008.10:g.143955843G>A , CM000670.1:g.143955843G>A	GRCh37
NC_000008.9:g.143952845G>A	NCBI36
NG_007954.1:g.10394C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1458C>T (CYP11B1) MANE Select	ENSP00000292427.5:p.Ser486=
ENST00000292427.8:c.1458C>T (CYP11B1)	ENSP00000292427.4:p.Ser486=
ENST00000314111.4:n.1655C>T (CYP11B1)
ENST00000377675.3:c.1671C>T (CYP11B1)	ENSP00000366903.3:p.Ser557=
ENST00000517471.5:c.1260C>T (CYP11B1)	ENSP00000428043.1:p.Ser420=
ENST00000519285.5:c.492C>T (CYP11B1)	ENSP00000430144.1:p.Ser164=
ENST00000522728.5:c.181+33202G>A (GML)	ENSP00000430799.1:n.181+33202G>A
NM_000497.3:c.1458C>T (CYP11B1)	NP_000488.3:p.Ser486=
NM_001026213.1:c.1260C>T (CYP11B1)	NP_001021384.1:p.Ser420=
XM_011516870.1:c.1696C>T (CYP11B1)	XP_011515172.1:p.Leu566Phe
XM_011516871.1:c.1627C>T (CYP11B1)	XP_011515173.1:p.Leu543Phe
XM_011516872.1:c.1618C>T (CYP11B1)	XP_011515174.1:p.Leu540Phe
XM_011516873.1:c.1605C>T (CYP11B1)	XP_011515175.1:p.Ser535=
XM_011516874.1:c.1536C>T (CYP11B1)	XP_011515176.1:p.Ser512=
XM_011516875.1:c.1435C>T (CYP11B1)	XP_011515177.1:p.Leu479Phe
XM_011516876.1:c.1407C>T (CYP11B1)	XP_011515178.1:p.Ser469=
XM_011516970.1:c.214+33202G>A (GML)	XP_011515272.1:n.214+33202G>A
NM_000497.4:c.1458C>T (CYP11B1) MANE Select	NP_000488.3:p.Ser486=