Canonical Allele Identifier: CA1021620999
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs779461255

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776792G>C , CM000683.2:g.28776792G>C GRCh38
NC_000021.8:g.30149114G>C , CM000683.1:g.30149114G>C GRCh37
NC_000021.7:g.29070985G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45113C>G
XR_002958591.1:n.4507-4654C>G