Canonical Allele Identifier: CA144309870
Gene:

Linked Data

dbSNP Id: rs773918687

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014467C>G , CM000668.2:g.98014467C>G GRCh38
NC_000006.11:g.98462343C>G , CM000668.1:g.98462343C>G GRCh37
NC_000006.10:g.98569064C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45001C>G
XR_942809.1:n.371+45001C>G