Canonical Allele Identifier: CA1825515650

Gene: CYP11B2 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914602_142914603delinsAC , CM000670.2:g.142914602_142914603delinsAC	GRCh38
NC_000008.10:g.143996018_143996019delinsAC , CM000670.1:g.143996018_143996019delinsAC	GRCh37
NC_000008.9:g.143993020_143993021delinsAC	NCBI36
NG_008374.1:g.8241_8242delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.799+102_799+103delinsGT (CYP11B2) MANE Select	ENSP00000325822.2:n.799+102_799+103delinsGT
ENST00000522728.5:c.264+557_264+558delinsAC (GML)	ENSP00000430799.1:n.264+557_264+558delinsAC
NM_000498.3:c.799+102_799+103delinsGT (CYP11B2) MANE Select	NP_000489.3:n.799+102_799+103delinsGT
XM_011516877.1:c.877+102_877+103delinsGT (CYP11B2)	XP_011515179.1:n.877+102_877+103delinsGT
XM_011516878.1:c.877+102_877+103delinsGT (CYP11B2)	XP_011515180.1:n.877+102_877+103delinsGT
XM_011516879.1:c.799+102_799+103delinsGT (CYP11B2)	XP_011515181.1:n.799+102_799+103delinsGT
XM_011516970.1:c.297+557_297+558delinsAC (GML)	XP_011515272.1:n.297+557_297+558delinsAC