Canonical Allele Identifier: CA1867363374
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs1830191811

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356793T>G , CM000671.2:g.99356793T>G GRCh38
NC_000009.11:g.102119075T>G , CM000671.1:g.102119075T>G GRCh37
NC_000009.10:g.101158896T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1191A>C
NR_102271.1:n.1419-1191A>C