Canonical Allele Identifier: CA2626674974
Gene: AMN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922669G>A , CM000676.2:g.102922669G>A GRCh38
NC_000014.8:g.103389006G>A , CM000676.1:g.103389006G>A GRCh37
NC_000014.7:g.102458759G>A NCBI36
NG_008276.2:g.5014G>A , LRG_642:g.5014G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.-20G>A MANE Select ENSP00000299155.6:n.-20G>A
ENST00000299155.9:c.-20G>A ENSP00000299155.5:n.-20G>A
NM_030943.3:c.-20G>A , LRG_642t1:c.-20G>A NP_112205.2:n.-20G>A
XM_011537202.1:c.-201G>A XP_011535504.1:n.-201G>A
XM_011537202.3:c.-201G>A XP_011535504.1:n.-201G>A
XM_024449714.1:c.77G>A XP_024305482.1:p.Gly26Asp
NM_030943.4:c.-20G>A MANE Select NP_112205.2:n.-20G>A