Canonical Allele Identifier: CA2688873379

Gene: CYP11B2 GML

Linked Data

• gnomAD v4: 8-142914560-G-GCCCCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914562_142914563insCCAACC , CM000670.2:g.142914562_142914563insCCAACC	GRCh38
NC_000008.10:g.143995978_143995979insCCAACC , CM000670.1:g.143995978_143995979insCCAACC	GRCh37
NC_000008.9:g.143992980_143992981insCCAACC	NCBI36
NG_008374.1:g.8283_8284insTTGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.800-143_800-142insTTGGGG (CYP11B2) MANE Select	ENSP00000325822.2:n.800-143_800-142insTTGGGG
ENST00000522728.5:c.264+517_264+518insCCAACC (GML)	ENSP00000430799.1:n.264+517_264+518insCCAACC
NM_000498.3:c.800-143_800-142insTTGGGG (CYP11B2) MANE Select	NP_000489.3:n.800-143_800-142insTTGGGG
XM_011516877.1:c.878-143_878-142insTTGGGG (CYP11B2)	XP_011515179.1:n.878-143_878-142insTTGGGG
XM_011516878.1:c.878-143_878-142insTTGGGG (CYP11B2)	XP_011515180.1:n.878-143_878-142insTTGGGG
XM_011516879.1:c.800-143_800-142insTTGGGG (CYP11B2)	XP_011515181.1:n.800-143_800-142insTTGGGG
XM_011516970.1:c.297+517_297+518insCCAACC (GML)	XP_011515272.1:n.297+517_297+518insCCAACC