Canonical Allele Identifier: CA2051430091
Gene:

Linked Data

dbSNP Id: rs1874796470

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84951898C>T , CM000674.2:g.84951898C>T GRCh38
NC_000012.11:g.85345677C>T , CM000674.1:g.85345677C>T GRCh37
NC_000012.10:g.83869808C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945152.1:n.316+30584C>T
XR_945153.1:n.301+13434C>T
XR_945154.1:n.174+37036C>T
XR_945155.1:n.330+30584C>T
XR_945152.2:n.316+30584C>T
XR_945154.2:n.174+37036C>T
XR_945155.2:n.888+30584C>T