Canonical Allele Identifier: CA2384891788
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1601044950

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776660G>A , CM000683.2:g.28776660G>A GRCh38
NC_000021.8:g.30148982G>A , CM000683.1:g.30148982G>A GRCh37
NC_000021.7:g.29070853G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45245C>T
XR_002958591.1:n.4507-4522C>T