Canonical Allele Identifier: CA319177677
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs898369182
MyVariant Identifiers: chr21:g.28776838C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776838C>T , CM000683.2:g.28776838C>T GRCh38
NC_000021.8:g.30149160C>T , CM000683.1:g.30149160C>T GRCh37
NC_000021.7:g.29071031C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45067G>A
XR_002958591.1:n.4507-4700G>A