Canonical Allele Identifier: CA1021621038
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1987298834

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776853T>C , CM000683.2:g.28776853T>C GRCh38
NC_000021.8:g.30149175T>C , CM000683.1:g.30149175T>C GRCh37
NC_000021.7:g.29071046T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45052A>G
XR_002958591.1:n.4507-4715A>G