Canonical Allele Identifier: CA372397328

Gene: CYP11B1 GML

Linked Data

• MyVariant Identifiers: chr8:g.143961118A>C (hg19) ; chr8:g.142879702A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142879702A>C , CM000670.2:g.142879702A>C	GRCh38
NC_000008.10:g.143961118A>C , CM000670.1:g.143961118A>C	GRCh37
NC_000008.9:g.143958120A>C	NCBI36
NG_007954.1:g.5119T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000292427.10:c.112T>G (CYP11B1) MANE Select	ENSP00000292427.5:p.Phe38Val
ENST00000292427.8:c.112T>G (CYP11B1)	ENSP00000292427.4:p.Phe38Val
ENST00000314111.4:n.145T>G (CYP11B1)
ENST00000377675.3:c.112T>G (CYP11B1)	ENSP00000366903.3:p.Phe38Val
ENST00000517471.5:c.112T>G (CYP11B1)	ENSP00000428043.1:p.Phe38Val
ENST00000522728.5:c.182-34261A>C (GML)	ENSP00000430799.1:n.182-34261A>C
NM_000497.3:c.112T>G (CYP11B1)	NP_000488.3:p.Phe38Val
NM_001026213.1:c.112T>G (CYP11B1)	NP_001021384.1:p.Phe38Val
XM_011516870.1:c.112T>G (CYP11B1)	XP_011515172.1:p.Phe38Val
XM_011516871.1:c.112T>G (CYP11B1)	XP_011515173.1:p.Phe38Val
XM_011516872.1:c.112T>G (CYP11B1)	XP_011515174.1:p.Phe38Val
XM_011516873.1:c.112T>G (CYP11B1)	XP_011515175.1:p.Phe38Val
XM_011516874.1:c.112T>G (CYP11B1)	XP_011515176.1:p.Phe38Val
XM_011516876.1:c.112T>G (CYP11B1)	XP_011515178.1:p.Phe38Val
XM_011516970.1:c.215-34261A>C (GML)	XP_011515272.1:n.215-34261A>C
NM_000497.4:c.112T>G (CYP11B1) MANE Select	NP_000488.3:p.Phe38Val