Canonical Allele Identifier: CA1021620972
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1568980314

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45141T>C
XR_002958591.1:n.4507-4626T>C