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Canonical Allele Identifier:
CA198901281
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806739T>C
GRCh37
chr9:g.117569019T>C
Linked Data - NCBI & NCI
dbSNP:
994559009
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806739T>C , CM000671.2:g.114806739T>C
GRCh38
NC_000009.11:g.117569019T>C , CM000671.1:g.117569019T>C
GRCh37
NC_000009.10:g.116608840T>C
NCBI36
NG_011488.2:g.4390A>G
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