Canonical Allele Identifier: CA2014002179
Gene:

Linked Data

dbSNP Id: rs1946882225

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6276599C>T , CM000674.2:g.6276599C>T GRCh38
NC_000012.11:g.6385765C>T , CM000674.1:g.6385765C>T GRCh37
NC_000012.10:g.6256026C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748976.1:n.157+16500G>A
XR_001748977.1:n.157+16500G>A
XR_001748978.1:n.157+16500G>A
XR_001748979.1:n.157+16500G>A
XR_001748980.1:n.157+16500G>A