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Canonical Allele Identifier:
CA815549885
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.92818872T>A
GRCh37
chr5:g.92154579T>A
Linked Data - NCBI & NCI
dbSNP:
17668565
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.92818872T>A , CM000667.2:g.92818872T>A
GRCh38
NC_000005.9:g.92154579T>A , CM000667.1:g.92154579T>A
GRCh37
NC_000005.8:g.92180335T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_948567.1:n.234+69650A>T
Search 100 bp 5'
Search 100 bp 3'