Canonical Allele Identifier: CA616397809
Gene: AMN HGNC NCBI

Linked Data

dbSNP Id: rs1463083992

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922629C>G , CM000676.2:g.102922629C>G GRCh38
NC_000014.8:g.103388966C>G , CM000676.1:g.103388966C>G GRCh37
NC_000014.7:g.102458719C>G NCBI36
NG_008276.2:g.4974C>G , LRG_642:g.4974C>G

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-241C>G XP_011535504.1:n.-241C>G
XM_011537202.3:c.-241C>G XP_011535504.1:n.-241C>G
XM_024449714.1:c.37C>G XP_024305482.1:p.Leu13Val