Canonical Allele Identifier: CA2160048468
Gene: AMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922636C= , CM000676.2:g.102922636C= GRCh38
NC_000014.8:g.103388973C= , CM000676.1:g.103388973C= GRCh37
NC_000014.7:g.102458726C= NCBI36
NG_008276.2:g.4981C= , LRG_642:g.4981C=

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-234C= XP_011535504.1:n.-234C=
XM_011537202.3:c.-234C= XP_011535504.1:n.-234C=
XM_024449714.1:c.44C= XP_024305482.1:p.Thr15=