Canonical Allele Identifier: CA716643701

Gene: AGBL1

Linked Data

• dbSNP Id: rs1467335992
• gnomAD v3: 15-86520897-C-G
• gnomAD v4: 15-86520897-C-G
• MyVariant Identifiers: chr15:g.87064128C>G (hg19) ; chr15:g.86520897C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.86520897C>G , CM000677.2:g.86520897C>G	GRCh38
NC_000015.9:g.87064128C>G , CM000677.1:g.87064128C>G	GRCh37
NC_000015.8:g.84865132C>G	NCBI36
NG_033836.1:g.383887C>G
NG_033836.2:g.446090C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000441037.7:c.2556-1913C>G	ENSP00000413001.3:n.2556-1913C>G
ENST00000614907.3:c.2556-1913C>G MANE Select	ENSP00000490608.2:n.2556-1913C>G
ENST00000421325.3:c.2418-1913C>G	ENSP00000397173.3:n.2418-1913C>G
ENST00000441037.6:c.2418-1913C>G	ENSP00000413001.2:n.2418-1913C>G
NM_152336.2:c.2418-1913C>G	NP_689549.2:n.2418-1913C>G
XM_011521226.1:c.2556-1913C>G	XP_011519528.1:n.2556-1913C>G
XM_011521227.1:c.2556-1913C>G	XP_011519529.1:n.2556-1913C>G
XR_931750.1:n.2597-1913C>G
NM_152336.3:c.2556-1913C>G	NP_689549.3:n.2556-1913C>G
XM_011521226.3:c.2556-1913C>G	XP_011519528.1:n.2556-1913C>G
XM_011521227.3:c.2556-1913C>G	XP_011519529.1:n.2556-1913C>G
XM_017021918.2:c.2523-1913C>G	XP_016877407.1:n.2523-1913C>G
XM_017021919.2:c.2472-1913C>G	XP_016877408.1:n.2472-1913C>G
XR_931750.3:n.2745-1913C>G
NM_152336.4:c.2556-1913C>G	NP_689549.3:n.2556-1913C>G
NM_001386094.1:c.2556-1913C>G MANE Select	NP_001373023.1:n.2556-1913C>G