Canonical Allele Identifier: CA319177518
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1006791065

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776604C>T , CM000683.2:g.28776604C>T GRCh38
NC_000021.8:g.30148926C>T , CM000683.1:g.30148926C>T GRCh37
NC_000021.7:g.29070797C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45301G>A
XR_002958591.1:n.4507-4466G>A