Canonical Allele Identifier: CA7359656

Gene: AMN

Linked Data

• dbSNP Id: rs746143548
• ExAC: 14:103388989 CAA / C
• gnomAD v2: 14-103388989-CAA-C
• gnomAD v3: 14-102922652-CAA-C
• gnomAD v4: 14-102922652-CAA-C
• MyVariant Identifiers: chr14:g.103388990_103388991del (hg19) ; chr14:g.102922653_102922654del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922654_102922655del , CM000676.2:g.102922654_102922655del	GRCh38
NC_000014.8:g.103388991_103388992del , CM000676.1:g.103388991_103388992del	GRCh37
NC_000014.7:g.102458744_102458745del	NCBI36
NG_008276.2:g.4999_5000del , LRG_642:g.4999_5000del

Transcript Alleles

HGVS	Amino-acid Change
XM_011537202.1:c.-216_-215del	XP_011535504.1:n.-216_-215del
XM_011537202.3:c.-216_-215del	XP_011535504.1:n.-216_-215del
XM_024449714.1:c.62_63del	XP_024305482.1:p.Lys21SerfsTer?