Canonical Allele Identifier: CA869139445

Gene: NAMA

Linked Data

• dbSNP Id: rs1019742187
• MyVariant Identifiers: chr9:g.102119146G>A (hg19) ; chr9:g.99356864G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356864G>A , CM000671.2:g.99356864G>A	GRCh38
NC_000009.11:g.102119146G>A , CM000671.1:g.102119146G>A	GRCh37
NC_000009.10:g.101158967G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1262C>T
NR_102271.1:n.1419-1262C>T