Canonical Allele Identifier: CA869139376

Gene: NAMA

Linked Data

• dbSNP Id: rs1490071267
• gnomAD v3: 9-99356786-G-T
• gnomAD v4: 9-99356786-G-T
• MyVariant Identifiers: chr9:g.102119068G>T (hg19) ; chr9:g.99356786G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356786G>T , CM000671.2:g.99356786G>T	GRCh38
NC_000009.11:g.102119068G>T , CM000671.1:g.102119068G>T	GRCh37
NC_000009.10:g.101158889G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1184C>A
NR_102271.1:n.1419-1184C>A