Canonical Allele Identifier: CA1825515571

Gene: CYP11B2 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914477_142914478delinsTC , CM000670.2:g.142914477_142914478delinsTC	GRCh38
NC_000008.10:g.143995893_143995894delinsTC , CM000670.1:g.143995893_143995894delinsTC	GRCh37
NC_000008.9:g.143992895_143992896delinsTC	NCBI36
NG_008374.1:g.8366_8367delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.800-60_800-59delinsGA (CYP11B2) MANE Select	ENSP00000325822.2:n.800-60_800-59delinsGA
ENST00000522728.5:c.264+432_264+433delinsTC (GML)	ENSP00000430799.1:n.264+432_264+433delinsTC
NM_000498.3:c.800-60_800-59delinsGA (CYP11B2) MANE Select	NP_000489.3:n.800-60_800-59delinsGA
XM_011516877.1:c.878-60_878-59delinsGA (CYP11B2)	XP_011515179.1:n.878-60_878-59delinsGA
XM_011516878.1:c.878-60_878-59delinsGA (CYP11B2)	XP_011515180.1:n.878-60_878-59delinsGA
XM_011516879.1:c.800-60_800-59delinsGA (CYP11B2)	XP_011515181.1:n.800-60_800-59delinsGA
XM_011516970.1:c.297+432_297+433delinsTC (GML)	XP_011515272.1:n.297+432_297+433delinsTC