Canonical Allele Identifier: CA2384891802
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1987296633

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776695G>A , CM000683.2:g.28776695G>A GRCh38
NC_000021.8:g.30149017G>A , CM000683.1:g.30149017G>A GRCh37
NC_000021.7:g.29070888G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45210C>T
XR_002958591.1:n.4507-4557C>T