Canonical Allele Identifier: CA319177497
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs551171348

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776575C>G , CM000683.2:g.28776575C>G GRCh38
NC_000021.8:g.30148897C>G , CM000683.1:g.30148897C>G GRCh37
NC_000021.7:g.29070768C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45330G>C
XR_002958591.1:n.4507-4437G>C