Canonical Allele Identifier: CA63405678
Gene:

Linked Data

dbSNP Id: rs773367623
MyVariant Identifiers: chr2:g.195871879C>A (hg19) chr2:g.195007155C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007155C>A , CM000664.2:g.195007155C>A GRCh38
NC_000002.11:g.195871879C>A , CM000664.1:g.195871879C>A GRCh37
NC_000002.10:g.195580124C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739836.1:n.553+52280G>T
Search 100 bp 5'
Search 100 bp 3'