Canonical Allele Identifier: CA319177615
Gene: N6AMT1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs144294997

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776737T>C , CM000683.2:g.28776737T>C GRCh38
NC_000021.8:g.30149059T>C , CM000683.1:g.30149059T>C GRCh37
NC_000021.7:g.29070930T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45168A>G
XR_002958591.1:n.4507-4599A>G