Canonical Allele Identifier: CA12914783
Gene:

Linked Data

dbSNP Id: rs10503951
gnomAD v2: 8-33665680-A-G
gnomAD v3: 8-33808162-A-G
gnomAD v4: 8-33808162-A-G
MyVariant Identifiers: chr8:g.33665680A>G (hg19) chr8:g.33808162A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808162A>G , CM000670.2:g.33808162A>G GRCh38
NC_000008.10:g.33665680A>G , CM000670.1:g.33665680A>G GRCh37
NC_000008.9:g.33785222A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949659.1:n.240+11726A>G
XR_002956701.1:n.240+11726A>G
Search 100 bp 5'
Search 100 bp 3'