Canonical Allele Identifier: CA2160048478
Gene: AMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922654A= , CM000676.2:g.102922654A= GRCh38
NC_000014.8:g.103388991A= , CM000676.1:g.103388991A= GRCh37
NC_000014.7:g.102458744A= NCBI36
NG_008276.2:g.4999A= , LRG_642:g.4999A=

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-216A= XP_011535504.1:n.-216A=
XM_011537202.3:c.-216A= XP_011535504.1:n.-216A=
XM_024449714.1:c.62A= XP_024305482.1:p.Lys21=