Canonical Allele Identifier: CA736559179

Gene: AGBL4

Linked Data

• dbSNP Id: rs1267330307
• gnomAD v3: 1-49719437-T-C
• gnomAD v4: 1-49719437-T-C
• MyVariant Identifiers: chr1:g.50185109T>C (hg19) ; chr1:g.49719437T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.49719437T>C , CM000663.2:g.49719437T>C	GRCh38
NC_000001.10:g.50185109T>C , CM000663.1:g.50185109T>C	GRCh37
NC_000001.9:g.49957696T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371839.6:c.158-22000A>G MANE Select	ENSP00000360905.1:n.158-22000A>G
ENST00000371836.1:c.158-22000A>G	ENSP00000360902.1:n.158-22000A>G
ENST00000371838.5:c.158-22000A>G	ENSP00000360904.1:n.158-22000A>G
ENST00000371839.5:c.158-22000A>G	ENSP00000360905.1:n.158-22000A>G
ENST00000497451.1:n.124-22000A>G
NM_032785.3:c.158-22000A>G	NP_116174.3:n.158-22000A>G
XM_006710986.2:c.158-22000A>G	XP_006711049.1:n.158-22000A>G
XM_011542308.1:c.158-22000A>G	XP_011540610.1:n.158-22000A>G
XM_011542309.1:c.158-22000A>G	XP_011540611.1:n.158-22000A>G
XM_011542310.1:c.158-22000A>G	XP_011540612.1:n.158-22000A>G
XM_011542311.1:c.158-22000A>G	XP_011540613.1:n.158-22000A>G
NM_001323573.1:c.158-22000A>G	NP_001310502.1:n.158-22000A>G
NM_001323574.1:c.158-22000A>G	NP_001310503.1:n.158-22000A>G
NM_001323575.1:c.158-22000A>G	NP_001310504.1:n.158-22000A>G
NR_136623.1:n.315+131959A>G
XM_011542308.2:c.158-22000A>G	XP_011540610.1:n.158-22000A>G
XM_011542310.2:c.158-22000A>G	XP_011540612.1:n.158-22000A>G
XM_017002595.2:c.158-22000A>G	XP_016858084.1:n.158-22000A>G
XM_017002596.2:c.158-22000A>G	XP_016858085.1:n.158-22000A>G
XM_017002597.2:c.158-22000A>G	XP_016858086.1:n.158-22000A>G
XM_017002598.2:c.158-22000A>G	XP_016858087.1:n.158-22000A>G
XM_024450399.1:c.158-22000A>G	XP_024306167.1:n.158-22000A>G
NM_032785.4:c.158-22000A>G MANE Select	NP_116174.3:n.158-22000A>G
NM_001323573.2:c.158-22000A>G	NP_001310502.1:n.158-22000A>G
NM_001323574.2:c.158-22000A>G	NP_001310503.1:n.158-22000A>G
NM_001323575.2:c.158-22000A>G	NP_001310504.1:n.158-22000A>G
NR_136623.2:n.315+131959A>G