Canonical Allele Identifier: CA154046039

Gene: AGMO

Linked Data

• dbSNP Id: rs1053726046
• gnomAD v3: 7-15455566-T-A
• gnomAD v4: 7-15455566-T-A
• MyVariant Identifiers: chr7:g.15495191T>A (hg19) ; chr7:g.15455566T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.15455566T>A , CM000669.2:g.15455566T>A	GRCh38
NC_000007.13:g.15495191T>A , CM000669.1:g.15495191T>A	GRCh37
NC_000007.12:g.15461716T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000342526.8:c.410-24458A>T MANE Select	ENSP00000341662.3:n.410-24458A>T
ENST00000342526.7:c.410-24458A>T	ENSP00000341662.3:n.410-24458A>T
NM_001004320.1:c.410-24458A>T	NP_001004320.1:n.410-24458A>T
XM_006715730.1:c.410-24458A>T	XP_006715793.1:n.410-24458A>T
XM_006715731.2:c.410-24458A>T	XP_006715794.1:n.410-24458A>T
XM_011515402.1:c.410-24458A>T	XP_011513704.1:n.410-24458A>T
XM_011515403.1:c.410-24458A>T	XP_011513705.1:n.410-24458A>T
XM_006715731.3:c.410-24458A>T	XP_006715794.1:n.410-24458A>T
XM_011515402.3:c.410-24458A>T	XP_011513704.1:n.410-24458A>T
XM_017012204.1:c.410-24458A>T	XP_016867693.1:n.410-24458A>T
XR_001744759.1:n.580-24458A>T
NM_001004320.2:c.410-24458A>T MANE Select	NP_001004320.1:n.410-24458A>T