Canonical Allele Identifier: CA915798044
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs1564295159
gnomAD v3: 9-99356817-A-G
gnomAD v4: 9-99356817-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356817A>G , CM000671.2:g.99356817A>G GRCh38
NC_000009.11:g.102119099A>G , CM000671.1:g.102119099A>G GRCh37
NC_000009.10:g.101158920A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1215T>C
NR_102271.1:n.1419-1215T>C