Canonical Allele Identifier: CA2352918737
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.17141948A>T , CM000682.2:g.17141948A>T GRCh38
NC_000020.10:g.17122593A>T , CM000682.1:g.17122593A>T GRCh37
NC_000020.9:g.17070593A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937288.1:n.310+6816A>T
XR_937289.1:n.310+6816A>T
XR_937288.2:n.310+6816A>T