Canonical Allele Identifier: CA183508219
Gene:

Linked Data

dbSNP Id: rs941769327
MyVariant Identifiers: chr8:g.108789848C>T (hg19) chr8:g.107777620C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.107777620C>T , CM000670.2:g.107777620C>T GRCh38
NC_000008.10:g.108789848C>T , CM000670.1:g.108789848C>T GRCh37
NC_000008.9:g.108859024C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928527.1:n.185+856G>A
XR_928527.2:n.219+856G>A
Search 100 bp 5'
Search 100 bp 3'