Canonical Allele Identifier: CA10655163
Gene:
MyVariant.info:
GRCh38 chr1:g.1070426C>T
GRCh37 chr1:g.1005806C>T
gnomAD v2:
1:1005806 C / T
gnomAD v3:
1:1070426 C / T
gnomAD v4:
chr1-1070426-C-T
Joint Max Group AF 0.31095959 (AFR)
Genomes Max Group AF 0.31095959 (AFR)
dbSNP:
3934834
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1070426C>T , CM000663.2:g.1070426C>T GRCh38
NC_000001.10:g.1005806C>T , CM000663.1:g.1005806C>T GRCh37
NC_000001.9:g.995669C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_024451970.1:c.-481G>A XP_024307738.1:n.-481G>A
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