Canonical Allele Identifier: CA202772641
Gene:

Linked Data

dbSNP Id: rs17144046
gnomAD v2: 10-8606014-A-G
gnomAD v3: 10-8564051-A-G
gnomAD v4: 10-8564051-A-G
MyVariant Identifiers: chr10:g.8606014A>G (hg19) chr10:g.8564051A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8564051A>G , CM000672.2:g.8564051A>G GRCh38
NC_000010.10:g.8606014A>G , CM000672.1:g.8606014A>G GRCh37
NC_000010.9:g.8646020A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930640.1:n.73-25237A>G
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