Canonical Allele Identifier: CA2051430376
Gene:

Linked Data

dbSNP Id: rs1874804456

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84952116A>C , CM000674.2:g.84952116A>C GRCh38
NC_000012.11:g.85345895A>C , CM000674.1:g.85345895A>C GRCh37
NC_000012.10:g.83870026A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945152.1:n.316+30802A>C
XR_945153.1:n.301+13652A>C
XR_945154.1:n.175-36826A>C
XR_945155.1:n.330+30802A>C
XR_945152.2:n.316+30802A>C
XR_945154.2:n.175-36826A>C
XR_945155.2:n.888+30802A>C