Canonical Allele Identifier: CA1649498387
Gene:

Linked Data

dbSNP Id: rs1772158841

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014816A>C , CM000668.2:g.98014816A>C GRCh38
NC_000006.11:g.98462692A>C , CM000668.1:g.98462692A>C GRCh37
NC_000006.10:g.98569413A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45350A>C
XR_942809.1:n.371+45350A>C