Canonical Allele Identifier: CA2626674719
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922613-C-A
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XM_011537202.1:c.-257C>A XP_011535504.1:n.-257C>A
XM_011537202.3:c.-257C>A XP_011535504.1:n.-257C>A
XM_024449714.1:c.21C>A XP_024305482.1:p.Cys7Ter
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