Canonical Allele Identifier: CA2626674815
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922633-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922633T>G , CM000676.2:g.102922633T>G GRCh38
NC_000014.8:g.103388970T>G , CM000676.1:g.103388970T>G GRCh37
NC_000014.7:g.102458723T>G NCBI36
NG_008276.2:g.4978T>G , LRG_642:g.4978T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-237T>G XP_011535504.1:n.-237T>G
XM_011537202.3:c.-237T>G XP_011535504.1:n.-237T>G
XM_024449714.1:c.41T>G XP_024305482.1:p.Val14Gly
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