Canonical Allele Identifier: CA1649534193
Gene:

Linked Data

dbSNP Id: rs1773158307

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102320G>C , CM000668.2:g.98102320G>C GRCh38
NC_000006.11:g.98550196G>C , CM000668.1:g.98550196G>C GRCh37
NC_000006.10:g.98656917G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.456+3050G>C
XR_942809.1:n.456+3050G>C