Canonical Allele Identifier: CA2769720757
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465996A>G , CM000668.2:g.465996A>G GRCh38
NC_000006.11:g.465996A>G , CM000668.1:g.465996A>G GRCh37
NC_000006.10:g.410996A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926364.1:n.2714+12271A>G
XR_926365.1:n.2548+12271A>G
XR_001743914.1:n.482-9212A>G