Canonical Allele Identifier: CA2160048467
Gene: AMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922635A= , CM000676.2:g.102922635A= GRCh38
NC_000014.8:g.103388972A= , CM000676.1:g.103388972A= GRCh37
NC_000014.7:g.102458725A= NCBI36
NG_008276.2:g.4980A= , LRG_642:g.4980A=

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-235A= XP_011535504.1:n.-235A=
XM_011537202.3:c.-235A= XP_011535504.1:n.-235A=
XM_024449714.1:c.43A= XP_024305482.1:p.Thr15=