Canonical Allele Identifier: CA2688873308

Gene: CYP11B2 GML

Linked Data

• gnomAD v4: 8-142914480-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914482del , CM000670.2:g.142914482del	GRCh38
NC_000008.10:g.143995898del , CM000670.1:g.143995898del	GRCh37
NC_000008.9:g.143992900del	NCBI36
NG_008374.1:g.8363del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.800-63del (CYP11B2) MANE Select	ENSP00000325822.2:n.800-63del
ENST00000522728.5:c.264+437del (GML)	ENSP00000430799.1:n.264+437del
NM_000498.3:c.800-63del (CYP11B2) MANE Select	NP_000489.3:n.800-63del
XM_011516877.1:c.878-63del (CYP11B2)	XP_011515179.1:n.878-63del
XM_011516878.1:c.878-63del (CYP11B2)	XP_011515180.1:n.878-63del
XM_011516879.1:c.800-63del (CYP11B2)	XP_011515181.1:n.800-63del
XM_011516970.1:c.297+437del (GML)	XP_011515272.1:n.297+437del