Canonical Allele Identifier: CA1867363353
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs1830191366

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356754C>T , CM000671.2:g.99356754C>T GRCh38
NC_000009.11:g.102119036C>T , CM000671.1:g.102119036C>T GRCh37
NC_000009.10:g.101158857C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1152G>A
NR_102271.1:n.1419-1152G>A