Canonical Allele Identifier: CA220638166

Gene:

Linked Data

• dbSNP Id: rs766522213
• MyVariant Identifiers: chr11:g.34780947T>G (hg19) ; chr11:g.34759400T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34759400T>G , CM000673.2:g.34759400T>G	GRCh38
NC_000011.9:g.34780947T>G , CM000673.1:g.34780947T>G	GRCh37
NC_000011.8:g.34737523T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+4793T>G
XR_931188.1:n.693+4793T>G
XR_931189.1:n.854+4793T>G
XR_931190.1:n.639+4793T>G
XR_931191.1:n.689+4793T>G
XR_001748174.1:n.855+4793T>G
XR_001748176.1:n.1016+4793T>G
XR_002957246.1:n.639+4793T>G