Canonical Allele Identifier: CA748443969
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1233067731
gnomAD v3: 21-28776839-G-A
gnomAD v4: 21-28776839-G-A
MyVariant Identifiers: chr21:g.30149161G>A (hg19) chr21:g.28776839G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776839G>A , CM000683.2:g.28776839G>A GRCh38
NC_000021.8:g.30149161G>A , CM000683.1:g.30149161G>A GRCh37
NC_000021.7:g.29071032G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45066C>T
XR_002958591.1:n.4507-4701C>T
Search 100 bp 5'
Search 100 bp 3'