Canonical Allele Identifier: CA966745625

Gene: AMN

Linked Data

• gnomAD v3: 14-102922612-GC-G
• gnomAD v4: 14-102922612-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922617del , CM000676.2:g.102922617del	GRCh38
NC_000014.8:g.103388954del , CM000676.1:g.103388954del	GRCh37
NC_000014.7:g.102458707del	NCBI36
NG_008276.2:g.4962del , LRG_642:g.4962del

Transcript Alleles

HGVS	Amino-acid Change
XM_011537202.1:c.-253del	XP_011535504.1:n.-253del
XM_011537202.3:c.-253del	XP_011535504.1:n.-253del
XM_024449714.1:c.25del	XP_024305482.1:p.His9ThrfsTer?