Canonical Allele Identifier: CA293120792
Gene:

Linked Data

dbSNP Id: rs1024002429

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240282C>T , CM000679.2:g.66240282C>T GRCh38
NC_000017.10:g.64236400C>T , CM000679.1:g.64236400C>T GRCh37
NC_000017.9:g.61666862C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10860G>A ENSP00000464301.1:p.=