Canonical Allele Identifier: CA2626674942
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922664-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922664G>A , CM000676.2:g.102922664G>A GRCh38
NC_000014.8:g.103389001G>A , CM000676.1:g.103389001G>A GRCh37
NC_000014.7:g.102458754G>A NCBI36
NG_008276.2:g.5009G>A , LRG_642:g.5009G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.-25G>A MANE Select ENSP00000299155.6:n.-25G>A
ENST00000299155.9:c.-25G>A ENSP00000299155.5:n.-25G>A
NM_030943.3:c.-25G>A , LRG_642t1:c.-25G>A NP_112205.2:n.-25G>A
XM_011537202.1:c.-206G>A XP_011535504.1:n.-206G>A
XM_011537202.3:c.-206G>A XP_011535504.1:n.-206G>A
XM_024449714.1:c.72G>A XP_024305482.1:p.Trp24Ter
NM_030943.4:c.-25G>A MANE Select NP_112205.2:n.-25G>A
Search 100 bp 5'
Search 100 bp 3'