Canonical Allele Identifier: CA1867363389
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs762734870

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356837G>C , CM000671.2:g.99356837G>C GRCh38
NC_000009.11:g.102119119G>C , CM000671.1:g.102119119G>C GRCh37
NC_000009.10:g.101158940G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1235C>G
NR_102271.1:n.1419-1235C>G