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Canonical Allele Identifier:
CA63790175
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203874146G>T
GRCh37
chr2:g.204738869G>T
Linked Data - Sequence & Population
gnomAD v3:
2:203874146 G / T
gnomAD v4:
chr2-203874146-G-T
Linked Data - NCBI & NCI
dbSNP:
35482731
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203874146G>T , CM000664.2:g.203874146G>T
GRCh38
NC_000002.11:g.204738869G>T , CM000664.1:g.204738869G>T
GRCh37
NC_000002.10:g.204447114G>T
NCBI36
NG_011502.1:g.11361G>T
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