Canonical Allele Identifier: CA2626674768
Gene: AMN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922622G>A , CM000676.2:g.102922622G>A GRCh38
NC_000014.8:g.103388959G>A , CM000676.1:g.103388959G>A GRCh37
NC_000014.7:g.102458712G>A NCBI36
NG_008276.2:g.4967G>A , LRG_642:g.4967G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-248G>A XP_011535504.1:n.-248G>A
XM_011537202.3:c.-248G>A XP_011535504.1:n.-248G>A
XM_024449714.1:c.30G>A XP_024305482.1:p.Pro10=