Canonical Allele Identifier: CA154046031

Gene: AGMO

Linked Data

• dbSNP Id: rs566333957
• gnomAD v2: 7-15495174-C-T
• gnomAD v3: 7-15455549-C-T
• gnomAD v4: 7-15455549-C-T
• MyVariant Identifiers: chr7:g.15495174C>T (hg19) ; chr7:g.15455549C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.15455549C>T , CM000669.2:g.15455549C>T	GRCh38
NC_000007.13:g.15495174C>T , CM000669.1:g.15495174C>T	GRCh37
NC_000007.12:g.15461699C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000342526.8:c.410-24441G>A MANE Select	ENSP00000341662.3:n.410-24441G>A
ENST00000342526.7:c.410-24441G>A	ENSP00000341662.3:n.410-24441G>A
NM_001004320.1:c.410-24441G>A	NP_001004320.1:n.410-24441G>A
XM_006715730.1:c.410-24441G>A	XP_006715793.1:n.410-24441G>A
XM_006715731.2:c.410-24441G>A	XP_006715794.1:n.410-24441G>A
XM_011515402.1:c.410-24441G>A	XP_011513704.1:n.410-24441G>A
XM_011515403.1:c.410-24441G>A	XP_011513705.1:n.410-24441G>A
XM_006715731.3:c.410-24441G>A	XP_006715794.1:n.410-24441G>A
XM_011515402.3:c.410-24441G>A	XP_011513704.1:n.410-24441G>A
XM_017012204.1:c.410-24441G>A	XP_016867693.1:n.410-24441G>A
XR_001744759.1:n.580-24441G>A
NM_001004320.2:c.410-24441G>A MANE Select	NP_001004320.1:n.410-24441G>A