Canonical Allele Identifier: CA675837331
Gene:

Linked Data

dbSNP Id: rs1332035885
gnomAD v3: 11-34759326-C-T
gnomAD v4: 11-34759326-C-T
MyVariant Identifiers: chr11:g.34780873C>T (hg19) chr11:g.34759326C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759326C>T , CM000673.2:g.34759326C>T GRCh38
NC_000011.9:g.34780873C>T , CM000673.1:g.34780873C>T GRCh37
NC_000011.8:g.34737449C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4719C>T
XR_931188.1:n.693+4719C>T
XR_931189.1:n.854+4719C>T
XR_931190.1:n.639+4719C>T
XR_931191.1:n.689+4719C>T
XR_001748174.1:n.855+4719C>T
XR_001748176.1:n.1016+4719C>T
XR_002957246.1:n.639+4719C>T
Search 100 bp 5'
Search 100 bp 3'