Canonical Allele Identifier: CA2573142970

Gene: CYP11B1 GML

Linked Data

• ClinVar Variation Id: 1653179
• ClinVar RCV Id: RCV002160923
• dbSNP Id: rs2130283816

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142879024C>A , CM000670.2:g.142879024C>A	GRCh38
NC_000008.10:g.143960440C>A , CM000670.1:g.143960440C>A	GRCh37
NC_000008.9:g.143957442C>A	NCBI36
NG_007954.1:g.5797G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.395+8G>T (CYP11B1) MANE Select	ENSP00000292427.5:n.395+8G>T
ENST00000292427.8:c.395+8G>T (CYP11B1)	ENSP00000292427.4:n.395+8G>T
ENST00000314111.4:n.428+8G>T (CYP11B1)
ENST00000377675.3:c.530+8G>T (CYP11B1)	ENSP00000366903.3:n.530+8G>T
ENST00000517471.5:c.395+8G>T (CYP11B1)	ENSP00000428043.1:n.395+8G>T
ENST00000522728.5:c.182-34939C>A (GML)	ENSP00000430799.1:n.182-34939C>A
NM_000497.3:c.395+8G>T (CYP11B1)	NP_000488.3:n.395+8G>T
NM_001026213.1:c.395+8G>T (CYP11B1)	NP_001021384.1:n.395+8G>T
XM_011516870.1:c.395+8G>T (CYP11B1)	XP_011515172.1:n.395+8G>T
XM_011516871.1:c.395+8G>T (CYP11B1)	XP_011515173.1:n.395+8G>T
XM_011516872.1:c.395+8G>T (CYP11B1)	XP_011515174.1:n.395+8G>T
XM_011516873.1:c.395+8G>T (CYP11B1)	XP_011515175.1:n.395+8G>T
XM_011516874.1:c.395+8G>T (CYP11B1)	XP_011515176.1:n.395+8G>T
XM_011516875.1:c.134+8G>T (CYP11B1)	XP_011515177.1:n.134+8G>T
XM_011516876.1:c.395+8G>T (CYP11B1)	XP_011515178.1:n.395+8G>T
XM_011516970.1:c.215-34939C>A (GML)	XP_011515272.1:n.215-34939C>A
NM_000497.4:c.395+8G>T (CYP11B1) MANE Select	NP_000488.3:n.395+8G>T