Canonical Allele Identifier: CA2581612307
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765645A>T , CM000668.2:g.163765645A>T GRCh38
NC_000006.11:g.164186677A>T , CM000668.1:g.164186677A>T GRCh37
NC_000006.10:g.164106667A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6216A>T
XR_001744454.1:n.369+6257A>T
XR_001744455.1:n.346+6280A>T