Canonical Allele Identifier: CA869139443

Gene: NAMA

Linked Data

• dbSNP Id: rs1480701955
• MyVariant Identifiers: chr9:g.102119142A>G (hg19) ; chr9:g.99356860A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356860A>G , CM000671.2:g.99356860A>G	GRCh38
NC_000009.11:g.102119142A>G , CM000671.1:g.102119142A>G	GRCh37
NC_000009.10:g.101158963A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1258T>C
NR_102271.1:n.1419-1258T>C