Canonical Allele Identifier: CA869139384

Gene: NAMA

Linked Data

• dbSNP Id: rs1286350590
• gnomAD v3: 9-99356787-A-C
• gnomAD v4: 9-99356787-A-C
• MyVariant Identifiers: chr9:g.102119069A>C (hg19) ; chr9:g.99356787A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356787A>C , CM000671.2:g.99356787A>C	GRCh38
NC_000009.11:g.102119069A>C , CM000671.1:g.102119069A>C	GRCh37
NC_000009.10:g.101158890A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1185T>G
NR_102271.1:n.1419-1185T>G