Canonical Allele Identifier: CA1867363365
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs1587737700

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356775T>G , CM000671.2:g.99356775T>G GRCh38
NC_000009.11:g.102119057T>G , CM000671.1:g.102119057T>G GRCh37
NC_000009.10:g.101158878T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1173A>C
NR_102271.1:n.1419-1173A>C