Canonical Allele Identifier: CA2626674690
Gene: AMN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922607C>T , CM000676.2:g.102922607C>T GRCh38
NC_000014.8:g.103388944C>T , CM000676.1:g.103388944C>T GRCh37
NC_000014.7:g.102458697C>T NCBI36
NG_008276.2:g.4952C>T , LRG_642:g.4952C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-263C>T XP_011535504.1:n.-263C>T
XM_011537202.3:c.-263C>T XP_011535504.1:n.-263C>T
XM_024449714.1:c.15C>T XP_024305482.1:p.Pro5=