Canonical Allele Identifier: CA211665909
Gene:

Linked Data

dbSNP Id: rs1015120537
gnomAD v3: 10-94762414-A-G
gnomAD v4: 10-94762414-A-G
MyVariant Identifiers: chr10:g.96522171A>G (hg19) chr10:g.94762414A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762414A>G , CM000672.2:g.94762414A>G GRCh38
NC_000010.10:g.96522171A>G , CM000672.1:g.96522171A>G GRCh37
NC_000010.9:g.96512161A>G NCBI36
NG_008384.2:g.4709A>G
NG_008384.3:g.4734A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12644A>G ENSP00000483243.1:n.932-12644A>G
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