Canonical Allele Identifier: CA197094493

Gene: NAMA

Linked Data

• dbSNP Id: rs562964059
• gnomAD v2: 9-102119105-C-A
• gnomAD v3: 9-99356823-C-A
• gnomAD v4: 9-99356823-C-A
• MyVariant Identifiers: chr9:g.102119105C>A (hg19) ; chr9:g.99356823C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356823C>A , CM000671.2:g.99356823C>A	GRCh38
NC_000009.11:g.102119105C>A , CM000671.1:g.102119105C>A	GRCh37
NC_000009.10:g.101158926C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1221G>T
NR_102271.1:n.1419-1221G>T