Canonical Allele Identifier: CA2160048450
Gene: AMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922613C= , CM000676.2:g.102922613C= GRCh38
NC_000014.8:g.103388950C= , CM000676.1:g.103388950C= GRCh37
NC_000014.7:g.102458703C= NCBI36
NG_008276.2:g.4958C= , LRG_642:g.4958C=

Transcript Alleles

HGVS Amino-acid change
XM_011537202.1:c.-257C= XP_011535504.1:n.-257C=
XM_011537202.3:c.-257C= XP_011535504.1:n.-257C=
XM_024449714.1:c.21C= XP_024305482.1:p.Cys7=