Canonical Allele Identifier: CA2160048480
Gene: AMN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922656G= , CM000676.2:g.102922656G= GRCh38
NC_000014.8:g.103388993G= , CM000676.1:g.103388993G= GRCh37
NC_000014.7:g.102458746G= NCBI36
NG_008276.2:g.5001G= , LRG_642:g.5001G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.9:c.-33G= ENSP00000299155.5:n.-33G=
NM_030943.3:c.-33G= , LRG_642t1:c.-33G= NP_112205.2:n.-33G=
XM_011537202.1:c.-214G= XP_011535504.1:n.-214G=
XM_011537202.3:c.-214G= XP_011535504.1:n.-214G=
XM_024449714.1:c.64G= XP_024305482.1:p.Val22=
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