Canonical Allele Identifier: CA2384891820
Gene: N6AMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776764A= , CM000683.2:g.28776764A= GRCh38
NC_000021.8:g.30149086A= , CM000683.1:g.30149086A= GRCh37
NC_000021.7:g.29070957A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45141T=
XR_002958591.1:n.4507-4626T=