Canonical Allele Identifier: CA2384891821
Gene: N6AMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776765T= , CM000683.2:g.28776765T= GRCh38
NC_000021.8:g.30149087T= , CM000683.1:g.30149087T= GRCh37
NC_000021.7:g.29070958T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45140A=
XR_002958591.1:n.4507-4627A=