Canonical Allele Identifier: CA2564980604
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072285G>T , CM000666.2:g.54072285G>T GRCh38
NC_000004.11:g.54938452G>T , CM000666.1:g.54938452G>T GRCh37
NC_000004.10:g.54633209G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202640G>T ENSP00000423325.1:n.1018-202640G>T