Canonical Allele Identifier: CA2769749871
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535736T>C , CM000668.2:g.1535736T>C GRCh38
NC_000006.11:g.1535971T>C , CM000668.1:g.1535971T>C GRCh37
NC_000006.10:g.1480970T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16610A>G
XR_926380.1:n.218-2720T>C
XR_926381.1:n.1108-2720T>C
XR_926382.1:n.235-6557A>G
XR_926384.1:n.200-6557A>G
XR_001743921.1:n.235-6581A>G
XR_427861.3:n.234+16610A>G
XR_926381.2:n.1123-2720T>C