Canonical Allele Identifier: CA675841049

Gene:

Linked Data

• dbSNP Id: rs1200098000
• MyVariant Identifiers: chr11:g.34834043A>C (hg19) ; chr11:g.34812496A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812496A>C , CM000673.2:g.34812496A>C	GRCh38
NC_000011.9:g.34834043A>C , CM000673.1:g.34834043A>C	GRCh37
NC_000011.8:g.34790619A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+57889A>C
XR_931188.1:n.693+57889A>C
XR_931189.1:n.854+57889A>C
XR_931190.1:n.639+57889A>C
XR_931191.1:n.689+57889A>C
XR_001748174.1:n.855+57889A>C
XR_001748176.1:n.1016+57889A>C
XR_002957246.1:n.639+57889A>C