Canonical Allele Identifier: CA106421622
Gene:
dbSNP:
10026364
gnomAD v2:
4:135522740 C / T
gnomAD v3:
4:134601585 C / T
gnomAD v4:
chr4-134601585-C-T
Joint Max Group AF 0.15414692 (AFR)
Genomes Max Group AF 0.15414692 (AFR)
MyVariant.info:
GRCh38 chr4:g.134601585C>T
GRCh37 chr4:g.135522740C>T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601585C>T , CM000666.2:g.134601585C>T GRCh38
NC_000004.11:g.135522740C>T , CM000666.1:g.135522740C>T GRCh37
NC_000004.10:g.135742190C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14226C>T
XR_939214.1:n.392+14226C>T
XR_939214.2:n.392+14226C>T
Search 100 bp 5'
Search 100 bp 3'