Canonical Allele Identifier: CA319177600

Gene: N6AMT1

Linked Data

• dbSNP Id: rs780234176
• MyVariant Identifiers: chr21:g.30149038C>G (hg19) ; chr21:g.28776716C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.28776716C>G , CM000683.2:g.28776716C>G	GRCh38
NC_000021.8:g.30149038C>G , CM000683.1:g.30149038C>G	GRCh37
NC_000021.7:g.29070909C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001754830.1:n.934+45189G>C
XR_002958591.1:n.4507-4578G>C