Canonical Allele Identifier: CA1127264235
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs1830191783
gnomAD v3: 9-99356788-C-A
gnomAD v4: 9-99356788-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356788C>A , CM000671.2:g.99356788C>A GRCh38
NC_000009.11:g.102119070C>A , CM000671.1:g.102119070C>A GRCh37
NC_000009.10:g.101158891C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1186G>T
NR_102271.1:n.1419-1186G>T
Search 100 bp 5'
Search 100 bp 3'