ClinGen Allele Registry
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Canonical Allele Identifier:
CA12291940
Gene: HLA-W
HGNC
NCBI
Linked Data
dbSNP Id:
rs892666
gnomAD v2:
6-29924728-T-C
gnomAD v3:
6-29956951-T-C
gnomAD v4:
6-29956951-T-C
MyVariant Identifiers:
chr6:g.29924728T>C (hg19)
chr6:g.29956951T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.29956951T>C , CM000668.2:g.29956951T>C
GRCh38
NC_000006.11:g.29924728T>C , CM000668.1:g.29924728T>C
GRCh37
NC_000006.10:g.30032707T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000439514.1:n.261+95T>C
Search 100 bp 5'
Search 100 bp 3'