Canonical Allele Identifier: CA319177516
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1002592176

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776585G>A , CM000683.2:g.28776585G>A GRCh38
NC_000021.8:g.30148907G>A , CM000683.1:g.30148907G>A GRCh37
NC_000021.7:g.29070778G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45320C>T
XR_002958591.1:n.4507-4447C>T