Canonical Allele Identifier: CA950002291
Gene:

Linked Data

dbSNP Id: rs1874806594

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84952169A>G , CM000674.2:g.84952169A>G GRCh38
NC_000012.11:g.85345948A>G , CM000674.1:g.85345948A>G GRCh37
NC_000012.10:g.83870079A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945152.1:n.316+30855A>G
XR_945153.1:n.301+13705A>G
XR_945154.1:n.175-36773A>G
XR_945155.1:n.330+30855A>G
XR_945152.2:n.316+30855A>G
XR_945154.2:n.175-36773A>G
XR_945155.2:n.888+30855A>G