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Canonical Allele Identifier:
CA31810418
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.163063928T>C
GRCh37
chr1:g.163033718T>C
Linked Data - Sequence & Population
gnomAD v3:
1:163063928 T / C
gnomAD v4:
chr1-163063928-T-C
Linked Data - NCBI & NCI
dbSNP:
906616498
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.163063928T>C , CM000663.2:g.163063928T>C
GRCh38
NC_000001.10:g.163033718T>C , CM000663.1:g.163033718T>C
GRCh37
NC_000001.9:g.161300342T>C
NCBI36
NG_023312.1:g.323T>C
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