Canonical Allele Identifier: CA2626674826
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922636-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922636C>A , CM000676.2:g.102922636C>A GRCh38
NC_000014.8:g.103388973C>A , CM000676.1:g.103388973C>A GRCh37
NC_000014.7:g.102458726C>A NCBI36
NG_008276.2:g.4981C>A , LRG_642:g.4981C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-234C>A XP_011535504.1:n.-234C>A
XM_011537202.3:c.-234C>A XP_011535504.1:n.-234C>A
XM_024449714.1:c.44C>A XP_024305482.1:p.Thr15Lys
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