Canonical Allele Identifier: CA267172352
Gene: AMN HGNC NCBI

Linked Data

dbSNP Id: rs958829979
gnomAD v4: 14-102922637-G-A
MyVariant Identifiers: chr14:g.103388974G>A (hg19) chr14:g.102922637G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922637G>A , CM000676.2:g.102922637G>A GRCh38
NC_000014.8:g.103388974G>A , CM000676.1:g.103388974G>A GRCh37
NC_000014.7:g.102458727G>A NCBI36
NG_008276.2:g.4982G>A , LRG_642:g.4982G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-233G>A XP_011535504.1:n.-233G>A
XM_011537202.3:c.-233G>A XP_011535504.1:n.-233G>A
XM_024449714.1:c.45G>A XP_024305482.1:p.Thr15=
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