Canonical Allele Identifier: CA2160048447
Gene: AMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922610G= , CM000676.2:g.102922610G= GRCh38
NC_000014.8:g.103388947G= , CM000676.1:g.103388947G= GRCh37
NC_000014.7:g.102458700G= NCBI36
NG_008276.2:g.4955G= , LRG_642:g.4955G=

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-260G= XP_011535504.1:n.-260G=
XM_011537202.3:c.-260G= XP_011535504.1:n.-260G=
XM_024449714.1:c.18G= XP_024305482.1:p.Trp6=