Canonical Allele Identifier: CA1649534202
Gene:

Linked Data

dbSNP Id: rs1773158421

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102339A>G , CM000668.2:g.98102339A>G GRCh38
NC_000006.11:g.98550215A>G , CM000668.1:g.98550215A>G GRCh37
NC_000006.10:g.98656936A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3069A>G
XR_942809.1:n.456+3069A>G