Canonical Allele Identifier: CA2626674891
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922652-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922652C>A , CM000676.2:g.102922652C>A GRCh38
NC_000014.8:g.103388989C>A , CM000676.1:g.103388989C>A GRCh37
NC_000014.7:g.102458742C>A NCBI36
NG_008276.2:g.4997C>A , LRG_642:g.4997C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-218C>A XP_011535504.1:n.-218C>A
XM_011537202.3:c.-218C>A XP_011535504.1:n.-218C>A
XM_024449714.1:c.60C>A XP_024305482.1:p.Gly20=
Search 100 bp 5'
Search 100 bp 3'