Canonical Allele Identifier: CA1825515708

Gene: CYP11B2 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914683_142914684delinsCT , CM000670.2:g.142914683_142914684delinsCT	GRCh38
NC_000008.10:g.143996099_143996100delinsCT , CM000670.1:g.143996099_143996100delinsCT	GRCh37
NC_000008.9:g.143993101_143993102delinsCT	NCBI36
NG_008374.1:g.8160_8161delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.799+21_799+22delinsAG (CYP11B2) MANE Select	ENSP00000325822.2:n.799+21_799+22delinsAG
ENST00000522728.5:c.264+638_264+639delinsCT (GML)	ENSP00000430799.1:n.264+638_264+639delinsCT
NM_000498.3:c.799+21_799+22delinsAG (CYP11B2) MANE Select	NP_000489.3:n.799+21_799+22delinsAG
XM_011516877.1:c.877+21_877+22delinsAG (CYP11B2)	XP_011515179.1:n.877+21_877+22delinsAG
XM_011516878.1:c.877+21_877+22delinsAG (CYP11B2)	XP_011515180.1:n.877+21_877+22delinsAG
XM_011516879.1:c.799+21_799+22delinsAG (CYP11B2)	XP_011515181.1:n.799+21_799+22delinsAG
XM_011516970.1:c.297+638_297+639delinsCT (GML)	XP_011515272.1:n.297+638_297+639delinsCT