Canonical Allele Identifier: CA319177513
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs144625650

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776576G>T , CM000683.2:g.28776576G>T GRCh38
NC_000021.8:g.30148898G>T , CM000683.1:g.30148898G>T GRCh37
NC_000021.7:g.29070769G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45329C>A
XR_002958591.1:n.4507-4438C>A