Canonical Allele Identifier: CA12190210
Gene: ETV7-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.36387877A>C
GRCh37 chr6:g.36355654A>C
gnomAD v2:
6:36355654 A / C
gnomAD v3:
6:36387877 A / C
gnomAD v4:
chr6-36387877-A-C
Joint Max Group AF 0.96740053 (AFR)
Genomes Max Group AF 0.9668709 (AFR)
Exomes Max Group AF 0.95548213 (AFR)
dbSNP:
2234067
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36387877A>C , CM000668.2:g.36387877A>C GRCh38
NC_000006.11:g.36355654A>C , CM000668.1:g.36355654A>C GRCh37
NC_000006.10:g.36463632A>C NCBI36
NG_029211.1:g.4924T>G

Transcript Alleles

HGVS Amino-acid Change
XR_926758.1:n.536+947A>C
XR_926758.2:n.89+947A>C
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