Canonical Allele Identifier: CA2626674926
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922661-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922661C>G , CM000676.2:g.102922661C>G GRCh38
NC_000014.8:g.103388998C>G , CM000676.1:g.103388998C>G GRCh37
NC_000014.7:g.102458751C>G NCBI36
NG_008276.2:g.5006C>G , LRG_642:g.5006C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.9:c.-28C>G ENSP00000299155.5:n.-28C>G
NM_030943.3:c.-28C>G , LRG_642t1:c.-28C>G NP_112205.2:n.-28C>G
XM_011537202.1:c.-209C>G XP_011535504.1:n.-209C>G
XM_011537202.3:c.-209C>G XP_011535504.1:n.-209C>G
XM_024449714.1:c.69C>G XP_024305482.1:p.Ser23=
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