Canonical Allele Identifier: CA15524287
Gene:
MyVariant.info:
GRCh38 chr7:g.24413286T>C
GRCh37 chr7:g.24452905T>C
gnomAD v2:
7:24452905 T / C
gnomAD v3:
7:24413286 T / C
gnomAD v4:
chr7-24413286-T-C
Joint Max Group AF 0.48355664 (EAS)
Genomes Max Group AF 0.48355664 (EAS)
dbSNP:
111
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24413286T>C , CM000669.2:g.24413286T>C GRCh38
NC_000007.13:g.24452905T>C , CM000669.1:g.24452905T>C GRCh37
NC_000007.12:g.24419430T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.-89+31773A>G XP_016868399.1:n.-89+31773A>G
XM_017012911.1:c.-89+31773A>G XP_016868400.1:n.-89+31773A>G
XR_001745121.1:n.344+31773A>G
XR_001745122.1:n.344+31773A>G
XR_001745123.1:n.344+31773A>G
XR_001745124.1:n.344+31773A>G
XR_001745125.1:n.344+31773A>G
XR_001745126.1:n.344+31773A>G
XR_001745127.1:n.344+31773A>G
XR_001745129.1:n.344+31773A>G
XR_001745130.1:n.344+31773A>G
XR_001745131.1:n.344+31773A>G
XR_001745132.1:n.344+31773A>G
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