Canonical Allele Identifier: CA1468682086
Gene:

Linked Data

dbSNP Id: rs1721060449

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74554007T>G , CM000666.2:g.74554007T>G GRCh38
NC_000004.11:g.75419724T>G , CM000666.1:g.75419724T>G GRCh37
NC_000004.10:g.75638588T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741513.1:n.167-1175A>C