Canonical Allele Identifier: CA13243799
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52743758A>C , CM000672.2:g.52743758A>C GRCh38
NC_000010.10:g.54503518A>C , CM000672.1:g.54503518A>C GRCh37
NC_000010.9:g.54173524A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945961.1:n.259+11548T>G
XR_945962.1:n.259+11548T>G
NR_155748.1:n.95+11552T>G
XR_945961.3:n.9306+11548T>G
XR_945962.3:n.9306+11548T>G