Canonical Allele Identifier: CA748443956

Gene: N6AMT1

Linked Data

• dbSNP Id: rs1395733484
• gnomAD v3: 21-28776669-A-C
• gnomAD v4: 21-28776669-A-C
• MyVariant Identifiers: chr21:g.30148991A>C (hg19) ; chr21:g.28776669A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.28776669A>C , CM000683.2:g.28776669A>C	GRCh38
NC_000021.8:g.30148991A>C , CM000683.1:g.30148991A>C	GRCh37
NC_000021.7:g.29070862A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001754830.1:n.934+45236T>G
XR_002958591.1:n.4507-4531T>G