ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA150162988
Gene:
Linked Data
dbSNP Id:
rs140068132
gnomAD v2:
6-151954834-A-G
gnomAD v3:
6-151633699-A-G
gnomAD v4:
6-151633699-A-G
MyVariant Identifiers:
chr6:g.151954834A>G (hg19)
chr6:g.151633699A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.151633699A>G , CM000668.2:g.151633699A>G
GRCh38
NC_000006.11:g.151954834A>G , CM000668.1:g.151954834A>G
GRCh37
NC_000006.10:g.151996527A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_943115.1:n.2496+3717A>G
Search 100 bp 5'
Search 100 bp 3'