Canonical Allele Identifier: CA1678638499
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765664A= , CM000668.2:g.163765664A= GRCh38
NC_000006.11:g.164186696A= , CM000668.1:g.164186696A= GRCh37
NC_000006.10:g.164106686A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6235A=
XR_001744454.1:n.369+6276A=
XR_001744455.1:n.346+6299A=