Canonical Allele Identifier: CA2706105101
Gene:

Linked Data

dbSNP Id: rs2110101348

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072438C>T , CM000666.2:g.54072438C>T GRCh38
NC_000004.11:g.54938605C>T , CM000666.1:g.54938605C>T GRCh37
NC_000004.10:g.54633362C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202487C>T ENSP00000423325.1:n.1018-202487C>T