ClinGen Allele Registry
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Canonical Allele Identifier:
CA15460028
Gene:
Linked Data
dbSNP Id:
rs1528983
gnomAD v2:
6-91544513-T-C
gnomAD v3:
6-90834795-T-C
gnomAD v4:
6-90834795-T-C
MyVariant Identifiers:
chr6:g.91544513T>C (hg19)
chr6:g.90834795T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.90834795T>C , CM000668.2:g.90834795T>C
GRCh38
NC_000006.11:g.91544513T>C , CM000668.1:g.91544513T>C
GRCh37
NC_000006.10:g.91601234T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_001744259.1:n.1244-73261T>C
Search 100 bp 5'
Search 100 bp 3'