Canonical Allele Identifier: CA1649498126
Gene:

Linked Data

dbSNP Id: rs1675189246

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014521G>C , CM000668.2:g.98014521G>C GRCh38
NC_000006.11:g.98462397G>C , CM000668.1:g.98462397G>C GRCh37
NC_000006.10:g.98569118G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45055G>C
XR_942809.1:n.371+45055G>C