Canonical Allele Identifier: CA2014002166
Gene:

Linked Data

dbSNP Id: rs1946882110

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6276566G>T , CM000674.2:g.6276566G>T GRCh38
NC_000012.11:g.6385732G>T , CM000674.1:g.6385732G>T GRCh37
NC_000012.10:g.6255993G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748976.1:n.157+16533C>A
XR_001748977.1:n.157+16533C>A
XR_001748978.1:n.157+16533C>A
XR_001748979.1:n.157+16533C>A
XR_001748980.1:n.157+16533C>A