Canonical Allele Identifier: CA319177463
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs549000814
gnomAD v3: 21-28776546-G-C
gnomAD v4: 21-28776546-G-C
MyVariant Identifiers: chr21:g.30148868G>C (hg19) chr21:g.28776546G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776546G>C , CM000683.2:g.28776546G>C GRCh38
NC_000021.8:g.30148868G>C , CM000683.1:g.30148868G>C GRCh37
NC_000021.7:g.29070739G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45359C>G
XR_002958591.1:n.4507-4408C>G
Search 100 bp 5'
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