Canonical Allele Identifier: CA15668641
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.120961461C>T , CM000672.2:g.120961461C>T GRCh38
NC_000010.10:g.122720974C>T , CM000672.1:g.122720974C>T GRCh37
NC_000010.9:g.122710964C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946372.1:n.99+19191G>A
XR_001747609.1:n.540+19191G>A
XR_946372.2:n.1002+19191G>A