Canonical Allele Identifier: CA2626674843
Gene: AMN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922639G>A , CM000676.2:g.102922639G>A GRCh38
NC_000014.8:g.103388976G>A , CM000676.1:g.103388976G>A GRCh37
NC_000014.7:g.102458729G>A NCBI36
NG_008276.2:g.4984G>A , LRG_642:g.4984G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-231G>A XP_011535504.1:n.-231G>A
XM_011537202.3:c.-231G>A XP_011535504.1:n.-231G>A
XM_024449714.1:c.47G>A XP_024305482.1:p.Trp16Ter