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Canonical Allele Identifier:
CA788742650
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.147361190T>A
GRCh37
chr4:g.148282342T>A
Linked Data - NCBI & NCI
dbSNP:
1429138
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.147361190T>A , CM000666.2:g.147361190T>A
GRCh38
NC_000004.11:g.148282342T>A , CM000666.1:g.148282342T>A
GRCh37
NC_000004.10:g.148501792T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'