Canonical Allele Identifier: CA1737807035
Gene:

Linked Data

dbSNP Id: rs1793587030

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.118519419C>T , CM000669.2:g.118519419C>T GRCh38
NC_000007.13:g.118159473C>T , CM000669.1:g.118159473C>T GRCh37
NC_000007.12:g.117946709C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927908.1:n.388+5592C>T
XR_927909.1:n.388+5592C>T
XR_927910.1:n.388+5592C>T
XR_927909.2:n.426+5592C>T