Canonical Allele Identifier: CA2712749628
Gene:

Linked Data

dbSNP Id: rs2127969086

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014477A>G , CM000668.2:g.98014477A>G GRCh38
NC_000006.11:g.98462353A>G , CM000668.1:g.98462353A>G GRCh37
NC_000006.10:g.98569074A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45011A>G
XR_942809.1:n.371+45011A>G