Canonical Allele Identifier: CA869139396

Gene: NAMA

Linked Data

• dbSNP Id: rs1353377650
• gnomAD v3: 9-99356798-C-T
• gnomAD v4: 9-99356798-C-T
• MyVariant Identifiers: chr9:g.102119080C>T (hg19) ; chr9:g.99356798C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356798C>T , CM000671.2:g.99356798C>T	GRCh38
NC_000009.11:g.102119080C>T , CM000671.1:g.102119080C>T	GRCh37
NC_000009.10:g.101158901C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1196G>A
NR_102271.1:n.1419-1196G>A