Canonical Allele Identifier: CA2716728508
Gene:

Linked Data

dbSNP Id: rs1804275096

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176601G>C , CM000670.2:g.31176601G>C GRCh38
NC_000008.10:g.31034117G>C , CM000670.1:g.31034117G>C GRCh37
NC_000008.9:g.31153659G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949642.1:n.270+12G>C
XR_949643.1:n.87+91C>G
XR_949644.1:n.87+91C>G
XR_949645.1:n.87+91C>G
XR_949646.1:n.87+91C>G
XR_949647.1:n.700+91C>G
XR_949648.1:n.602+91C>G