Canonical Allele Identifier: CA197094490
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs957978749
gnomAD v2: 9-102119078-C-G
gnomAD v3: 9-99356796-C-G
gnomAD v4: 9-99356796-C-G
MyVariant Identifiers: chr9:g.102119078C>G (hg19) chr9:g.99356796C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356796C>G , CM000671.2:g.99356796C>G GRCh38
NC_000009.11:g.102119078C>G , CM000671.1:g.102119078C>G GRCh37
NC_000009.10:g.101158899C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1194G>C
NR_102271.1:n.1419-1194G>C
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