Canonical Allele Identifier: CA1021620969
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1987297319

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776761C>G , CM000683.2:g.28776761C>G GRCh38
NC_000021.8:g.30149083C>G , CM000683.1:g.30149083C>G GRCh37
NC_000021.7:g.29070954C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45144G>C
XR_002958591.1:n.4507-4623G>C