Canonical Allele Identifier: CA869139436

Gene: NAMA

Linked Data

• dbSNP Id: rs1157792019
• MyVariant Identifiers: chr9:g.102119141G>A (hg19) ; chr9:g.99356859G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356859G>A , CM000671.2:g.99356859G>A	GRCh38
NC_000009.11:g.102119141G>A , CM000671.1:g.102119141G>A	GRCh37
NC_000009.10:g.101158962G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1257C>T
NR_102271.1:n.1419-1257C>T