Canonical Allele Identifier: CA2160048479
Gene: AMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922655A= , CM000676.2:g.102922655A= GRCh38
NC_000014.8:g.103388992A= , CM000676.1:g.103388992A= GRCh37
NC_000014.7:g.102458745A= NCBI36
NG_008276.2:g.5000A= , LRG_642:g.5000A=

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-215A= XP_011535504.1:n.-215A=
XM_011537202.3:c.-215A= XP_011535504.1:n.-215A=
XM_024449714.1:c.63A= XP_024305482.1:p.Lys21=