Canonical Allele Identifier: CA2626674484
Gene: AMN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922569_102922616del , CM000676.2:g.102922569_102922616del GRCh38
NC_000014.8:g.103388906_103388953del , CM000676.1:g.103388906_103388953del GRCh37
NC_000014.7:g.102458659_102458706del NCBI36
NG_008276.2:g.4914_4961del , LRG_642:g.4914_4961del

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-301_-254del XP_011535504.1:n.-301_-254del
XM_011537202.3:c.-301_-254del XP_011535504.1:n.-301_-254del
XM_024449714.1:c.-24_24del