Canonical Allele Identifier: CA1021620905
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1987295032

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776587G>A , CM000683.2:g.28776587G>A GRCh38
NC_000021.8:g.30148909G>A , CM000683.1:g.30148909G>A GRCh37
NC_000021.7:g.29070780G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45318C>T
XR_002958591.1:n.4507-4449C>T