Canonical Allele Identifier: CA1867363397
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs1830193194
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356857C>T , CM000671.2:g.99356857C>T GRCh38
NC_000009.11:g.102119139C>T , CM000671.1:g.102119139C>T GRCh37
NC_000009.10:g.101158960C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1255G>A
NR_102271.1:n.1419-1255G>A
Search 100 bp 5'
Search 100 bp 3'