Canonical Allele Identifier: CA2626674857
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922643-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922643C>T , CM000676.2:g.102922643C>T GRCh38
NC_000014.8:g.103388980C>T , CM000676.1:g.103388980C>T GRCh37
NC_000014.7:g.102458733C>T NCBI36
NG_008276.2:g.4988C>T , LRG_642:g.4988C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-227C>T XP_011535504.1:n.-227C>T
XM_011537202.3:c.-227C>T XP_011535504.1:n.-227C>T
XM_024449714.1:c.51C>T XP_024305482.1:p.Val17=
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