Canonical Allele Identifier: CA197094491

Gene: NAMA

Linked Data

• dbSNP Id: rs764641420
• gnomAD v3: 9-99356806-C-G
• gnomAD v4: 9-99356806-C-G
• MyVariant Identifiers: chr9:g.102119088C>G (hg19) ; chr9:g.99356806C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356806C>G , CM000671.2:g.99356806C>G	GRCh38
NC_000009.11:g.102119088C>G , CM000671.1:g.102119088C>G	GRCh37
NC_000009.10:g.101158909C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1204G>C
NR_102271.1:n.1419-1204G>C