Canonical Allele Identifier: CA572839322

Gene: AGMO

Linked Data

• dbSNP Id: rs1346374926
• gnomAD v2: 7-15495179-A-C
• gnomAD v3: 7-15455554-A-C
• gnomAD v4: 7-15455554-A-C
• MyVariant Identifiers: chr7:g.15495179A>C (hg19) ; chr7:g.15455554A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.15455554A>C , CM000669.2:g.15455554A>C	GRCh38
NC_000007.13:g.15495179A>C , CM000669.1:g.15495179A>C	GRCh37
NC_000007.12:g.15461704A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342526.8:c.410-24446T>G MANE Select	ENSP00000341662.3:n.410-24446T>G
ENST00000342526.7:c.410-24446T>G	ENSP00000341662.3:n.410-24446T>G
NM_001004320.1:c.410-24446T>G	NP_001004320.1:n.410-24446T>G
XM_006715730.1:c.410-24446T>G	XP_006715793.1:n.410-24446T>G
XM_006715731.2:c.410-24446T>G	XP_006715794.1:n.410-24446T>G
XM_011515402.1:c.410-24446T>G	XP_011513704.1:n.410-24446T>G
XM_011515403.1:c.410-24446T>G	XP_011513705.1:n.410-24446T>G
XM_006715731.3:c.410-24446T>G	XP_006715794.1:n.410-24446T>G
XM_011515402.3:c.410-24446T>G	XP_011513704.1:n.410-24446T>G
XM_017012204.1:c.410-24446T>G	XP_016867693.1:n.410-24446T>G
XR_001744759.1:n.580-24446T>G
NM_001004320.2:c.410-24446T>G MANE Select	NP_001004320.1:n.410-24446T>G