Canonical Allele Identifier: CA372395396

Gene: CYP11B1 GML

Linked Data

• MyVariant Identifiers: chr8:g.143958108G>C (hg19) ; chr8:g.142876692G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876692G>C , CM000670.2:g.142876692G>C	GRCh38
NC_000008.10:g.143958108G>C , CM000670.1:g.143958108G>C	GRCh37
NC_000008.9:g.143955110G>C	NCBI36
NG_007954.1:g.8129C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.789C>G (CYP11B1) MANE Select	ENSP00000292427.5:p.Ile263Met
ENST00000292427.8:c.789C>G (CYP11B1)	ENSP00000292427.4:p.Ile263Met
ENST00000314111.4:n.822C>G (CYP11B1)
ENST00000377675.3:c.1002C>G (CYP11B1)	ENSP00000366903.3:p.Ile334Met
ENST00000517471.5:c.789C>G (CYP11B1)	ENSP00000428043.1:p.Ile263Met
ENST00000522728.5:c.181+35467G>C (GML)	ENSP00000430799.1:n.181+35467G>C
NM_000497.3:c.789C>G (CYP11B1)	NP_000488.3:p.Ile263Met
NM_001026213.1:c.789C>G (CYP11B1)	NP_001021384.1:p.Ile263Met
XM_011516870.1:c.867C>G (CYP11B1)	XP_011515172.1:p.Ile289Met
XM_011516871.1:c.867C>G (CYP11B1)	XP_011515173.1:p.Ile289Met
XM_011516872.1:c.789C>G (CYP11B1)	XP_011515174.1:p.Ile263Met
XM_011516873.1:c.867C>G (CYP11B1)	XP_011515175.1:p.Ile289Met
XM_011516874.1:c.867C>G (CYP11B1)	XP_011515176.1:p.Ile289Met
XM_011516875.1:c.606C>G (CYP11B1)	XP_011515177.1:p.Ile202Met
XM_011516876.1:c.867C>G (CYP11B1)	XP_011515178.1:p.Ile289Met
XM_011516970.1:c.214+35467G>C (GML)	XP_011515272.1:n.214+35467G>C
NM_000497.4:c.789C>G (CYP11B1) MANE Select	NP_000488.3:p.Ile263Met