Canonical Allele Identifier: CA2160048482
Gene: AMN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922659T= , CM000676.2:g.102922659T= GRCh38
NC_000014.8:g.103388996T= , CM000676.1:g.103388996T= GRCh37
NC_000014.7:g.102458749T= NCBI36
NG_008276.2:g.5004T= , LRG_642:g.5004T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.9:c.-30T= ENSP00000299155.5:n.-30T=
NM_030943.3:c.-30T= , LRG_642t1:c.-30T= NP_112205.2:n.-30T=
XM_011537202.1:c.-211T= XP_011535504.1:n.-211T=
XM_011537202.3:c.-211T= XP_011535504.1:n.-211T=
XM_024449714.1:c.67T= XP_024305482.1:p.Ser23=
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