Canonical Allele Identifier: CA12796015
Gene:

Linked Data

dbSNP Id: rs4534106
gnomAD v2: 8-108789816-T-C
gnomAD v3: 8-107777588-T-C
gnomAD v4: 8-107777588-T-C
MyVariant Identifiers: chr8:g.108789816T>C (hg19) chr8:g.107777588T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.107777588T>C , CM000670.2:g.107777588T>C GRCh38
NC_000008.10:g.108789816T>C , CM000670.1:g.108789816T>C GRCh37
NC_000008.9:g.108858992T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928527.1:n.185+888A>G
XR_928527.2:n.219+888A>G
Search 100 bp 5'
Search 100 bp 3'