Canonical Allele Identifier: CA229981155

Gene:

Linked Data

• dbSNP Id: rs1038096243
• MyVariant Identifiers: chr11:g.116072593G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116072593G>C , CM000673.2:g.116072593G>C	GRCh38
NC_000011.9:g.115943311G>C , CM000673.1:g.115943311G>C	GRCh37
NC_000011.8:g.115448521G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948055.1:n.192+421C>G
XR_948056.1:n.311-5388C>G
XR_948057.1:n.97+516C>G
XR_001748401.1:n.192+421C>G
XR_948055.2:n.192+421C>G
XR_948056.2:n.314-5388C>G
XR_948057.2:n.97+516C>G