Canonical Allele Identifier: CA229981161
Gene:

Linked Data

dbSNP Id: rs903428227
gnomAD v3: 11-116072615-G-A
gnomAD v4: 11-116072615-G-A
MyVariant Identifiers: chr11:g.115943333G>A (hg19) chr11:g.116072615G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072615G>A , CM000673.2:g.116072615G>A GRCh38
NC_000011.9:g.115943333G>A , CM000673.1:g.115943333G>A GRCh37
NC_000011.8:g.115448543G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948055.1:n.192+399C>T
XR_948056.1:n.311-5410C>T
XR_948057.1:n.97+494C>T
XR_001748401.1:n.192+399C>T
XR_948055.2:n.192+399C>T
XR_948056.2:n.314-5410C>T
XR_948057.2:n.97+494C>T
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