Canonical Allele Identifier: CA177883267
Gene:

Linked Data

dbSNP Id: rs994880434
MyVariant Identifiers: chr8:g.58840849C>A (hg19) chr8:g.57928290C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.57928290C>A , CM000670.2:g.57928290C>A GRCh38
NC_000008.10:g.58840849C>A , CM000670.1:g.58840849C>A GRCh37
NC_000008.9:g.59003403C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928921.1:n.347-29986C>A
XR_928921.2:n.349-29986C>A
Search 100 bp 5'
Search 100 bp 3'