Canonical Allele Identifier: CA12184800
Gene: SLC17A1 HGNC NCBI

Linked Data

dbSNP Id: rs9467596
gnomAD v2: 6-25783022-T-C
gnomAD v3: 6-25782794-T-C
gnomAD v4: 6-25782794-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25782794T>C , CM000668.2:g.25782794T>C GRCh38
NC_000006.11:g.25783022T>C , CM000668.1:g.25783022T>C GRCh37
NC_000006.10:g.25891001T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011514818.1:c.*253A>G XP_011513120.1:n.*253A>G
XM_017011201.2:c.*2+15989A>G XP_016866690.1:n.*2+15989A>G