Canonical Allele Identifier: CA319177480
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs113175532
gnomAD v2: 21-30148890-A-T
gnomAD v3: 21-28776568-A-T
gnomAD v4: 21-28776568-A-T
MyVariant Identifiers: chr21:g.30148890A>T (hg19) chr21:g.28776568A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776568A>T , CM000683.2:g.28776568A>T GRCh38
NC_000021.8:g.30148890A>T , CM000683.1:g.30148890A>T GRCh37
NC_000021.7:g.29070761A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45337T>A
XR_002958591.1:n.4507-4430T>A
Search 100 bp 5'
Search 100 bp 3'