Canonical Allele Identifier: CA2160048454
Gene: AMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922617C= , CM000676.2:g.102922617C= GRCh38
NC_000014.8:g.103388954C= , CM000676.1:g.103388954C= GRCh37
NC_000014.7:g.102458707C= NCBI36
NG_008276.2:g.4962C= , LRG_642:g.4962C=

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-253C= XP_011535504.1:n.-253C=
XM_011537202.3:c.-253C= XP_011535504.1:n.-253C=
XM_024449714.1:c.25C= XP_024305482.1:p.His9=