Canonical Allele Identifier: CA2160048483
Gene: AMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922661C= , CM000676.2:g.102922661C= GRCh38
NC_000014.8:g.103388998C= , CM000676.1:g.103388998C= GRCh37
NC_000014.7:g.102458751C= NCBI36
NG_008276.2:g.5006C= , LRG_642:g.5006C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.9:c.-28C= ENSP00000299155.5:n.-28C=
NM_030943.3:c.-28C= , LRG_642t1:c.-28C= NP_112205.2:n.-28C=
XM_011537202.1:c.-209C= XP_011535504.1:n.-209C=
XM_011537202.3:c.-209C= XP_011535504.1:n.-209C=
XM_024449714.1:c.69C= XP_024305482.1:p.Ser23=