Canonical Allele Identifier: CA185200464
Gene:

Linked Data

dbSNP Id: rs973069624
MyVariant Identifiers: chr8:g.123408559T>C (hg19) chr8:g.122396320T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396320T>C , CM000670.2:g.122396320T>C GRCh38
NC_000008.10:g.123408559T>C , CM000670.1:g.123408559T>C GRCh37
NC_000008.9:g.123477740T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+2852A>G
XR_928599.3:n.152+2852A>G
Search 100 bp 5'
Search 100 bp 3'