Canonical Allele Identifier: CA2384891800
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1987296591

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776693A>C , CM000683.2:g.28776693A>C GRCh38
NC_000021.8:g.30149015A>C , CM000683.1:g.30149015A>C GRCh37
NC_000021.7:g.29070886A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45212T>G
XR_002958591.1:n.4507-4555T>G