Canonical Allele Identifier: CA2160048465
Gene: AMN HGNC NCBI

Linked Data

dbSNP Id: rs1595429493
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922630T>G , CM000676.2:g.102922630T>G GRCh38
NC_000014.8:g.103388967T>G , CM000676.1:g.103388967T>G GRCh37
NC_000014.7:g.102458720T>G NCBI36
NG_008276.2:g.4975T>G , LRG_642:g.4975T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-240T>G XP_011535504.1:n.-240T>G
XM_011537202.3:c.-240T>G XP_011535504.1:n.-240T>G
XM_024449714.1:c.38T>G XP_024305482.1:p.Leu13Arg
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