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Canonical Allele Identifier:
CA98367564
Gene:
Linked Data
dbSNP Id:
rs1017550060
MyVariant Identifiers:
chr4:g.62558184G>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.62558184G>T , CM000666.2:g.62558184G>T
GRCh38
NC_000004.11:g.63423902G>T , CM000666.1:g.63423902G>T
GRCh37
NC_000004.10:g.63106497G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_938814.1:n.161-5660G>T
Search 100 bp 5'
Search 100 bp 3'