Canonical Allele Identifier: CA319177699

Gene: N6AMT1

Linked Data

• dbSNP Id: rs907024219
• gnomAD v2: 21-30149219-A-G
• gnomAD v3: 21-28776897-A-G
• gnomAD v4: 21-28776897-A-G
• MyVariant Identifiers: chr21:g.30149219A>G (hg19) ; chr21:g.28776897A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.28776897A>G , CM000683.2:g.28776897A>G	GRCh38
NC_000021.8:g.30149219A>G , CM000683.1:g.30149219A>G	GRCh37
NC_000021.7:g.29071090A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001754830.1:n.934+45008T>C
XR_002958591.1:n.4507-4759T>C