Canonical Allele Identifier: CA1649498189
Gene:

Linked Data

dbSNP Id: rs1772156603

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014610C>G , CM000668.2:g.98014610C>G GRCh38
NC_000006.11:g.98462486C>G , CM000668.1:g.98462486C>G GRCh37
NC_000006.10:g.98569207C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45144C>G
XR_942809.1:n.371+45144C>G