Canonical Allele Identifier: CA2626674671
Gene: AMN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922604A>T , CM000676.2:g.102922604A>T GRCh38
NC_000014.8:g.103388941A>T , CM000676.1:g.103388941A>T GRCh37
NC_000014.7:g.102458694A>T NCBI36
NG_008276.2:g.4949A>T , LRG_642:g.4949A>T

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-266A>T XP_011535504.1:n.-266A>T
XM_011537202.3:c.-266A>T XP_011535504.1:n.-266A>T
XM_024449714.1:c.12A>T XP_024305482.1:p.Arg4=