Canonical Allele Identifier: CA1678638514
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765694T= , CM000668.2:g.163765694T= GRCh38
NC_000006.11:g.164186726T= , CM000668.1:g.164186726T= GRCh37
NC_000006.10:g.164106716T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6265T=
XR_001744454.1:n.369+6306T=
XR_001744455.1:n.346+6329T=