Canonical Allele Identifier: CA319177622
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs543660141

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776754T>G , CM000683.2:g.28776754T>G GRCh38
NC_000021.8:g.30149076T>G , CM000683.1:g.30149076T>G GRCh37
NC_000021.7:g.29070947T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45151A>C
XR_002958591.1:n.4507-4616A>C