Canonical Allele Identifier: CA220638188
Gene:

Linked Data

dbSNP Id: rs779001612
gnomAD v2: 11-34781107-G-A
gnomAD v3: 11-34759560-G-A
gnomAD v4: 11-34759560-G-A
MyVariant Identifiers: chr11:g.34781107G>A (hg19) chr11:g.34759560G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759560G>A , CM000673.2:g.34759560G>A GRCh38
NC_000011.9:g.34781107G>A , CM000673.1:g.34781107G>A GRCh37
NC_000011.8:g.34737683G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4953G>A
XR_931188.1:n.693+4953G>A
XR_931189.1:n.854+4953G>A
XR_931190.1:n.639+4953G>A
XR_931191.1:n.689+4953G>A
XR_001748174.1:n.855+4953G>A
XR_001748176.1:n.1016+4953G>A
XR_002957246.1:n.639+4953G>A
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