Canonical Allele Identifier: CA177883265
Gene:

Linked Data

dbSNP Id: rs1038176088
MyVariant Identifiers: chr8:g.58840830T>C (hg19) chr8:g.57928271T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.57928271T>C , CM000670.2:g.57928271T>C GRCh38
NC_000008.10:g.58840830T>C , CM000670.1:g.58840830T>C GRCh37
NC_000008.9:g.59003384T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928921.1:n.347-30005T>C
XR_928921.2:n.349-30005T>C
Search 100 bp 5'
Search 100 bp 3'