Canonical Allele Identifier: CA2839515301
Gene: AMN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922630del , CM000676.2:g.102922630del GRCh38
NC_000014.8:g.103388967del , CM000676.1:g.103388967del GRCh37
NC_000014.7:g.102458720del NCBI36
NG_008276.2:g.4975del , LRG_642:g.4975del

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-240del XP_011535504.1:n.-240del
XM_011537202.3:c.-240del XP_011535504.1:n.-240del
XM_024449714.1:c.38del XP_024305482.1:p.Leu13ArgfsTer?
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