Canonical Allele Identifier: CA2160048473
Gene: AMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922646G= , CM000676.2:g.102922646G= GRCh38
NC_000014.8:g.103388983G= , CM000676.1:g.103388983G= GRCh37
NC_000014.7:g.102458736G= NCBI36
NG_008276.2:g.4991G= , LRG_642:g.4991G=

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-224G= XP_011535504.1:n.-224G=
XM_011537202.3:c.-224G= XP_011535504.1:n.-224G=
XM_024449714.1:c.54G= XP_024305482.1:p.Gln18=