Canonical Allele Identifier: CA2544747532
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369167T>C , CM000664.2:g.122369167T>C GRCh38
NC_000002.11:g.123126743T>C , CM000664.1:g.123126743T>C GRCh37
NC_000002.10:g.122843213T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23796T>C
XR_001739684.1:n.556-23796T>C