Canonical Allele Identifier: CA197094496
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs766226205
gnomAD v2: 9-102119147-C-T
gnomAD v3: 9-99356865-C-T
gnomAD v4: 9-99356865-C-T
MyVariant Identifiers: chr9:g.102119147C>T (hg19) chr9:g.99356865C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356865C>T , CM000671.2:g.99356865C>T GRCh38
NC_000009.11:g.102119147C>T , CM000671.1:g.102119147C>T GRCh37
NC_000009.10:g.101158968C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1263G>A
NR_102271.1:n.1419-1263G>A
Search 100 bp 5'
Search 100 bp 3'