Canonical Allele Identifier: CA12229859
Gene:
dbSNP:
9259013
gnomAD v2:
6:29842467 T / A
gnomAD v3:
6:29874690 T / A
gnomAD v4:
chr6-29874690-T-A
Joint Max Group AF 0.96403638 (EAS)
Genomes Max Group AF 0.96403638 (EAS)
MyVariant.info:
GRCh38 chr6:g.29874690T>A
GRCh37 chr6:g.29842467T>A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29874690T>A , CM000668.2:g.29874690T>A GRCh38
NC_000006.11:g.29842467T>A , CM000668.1:g.29842467T>A GRCh37
NC_000006.10:g.29950446T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000647952.1:n.2062+8864A>T
Search 100 bp 5'
Search 100 bp 3'