Canonical Allele Identifier: CA2637311338
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880803G>T , CM000679.2:g.35880803G>T GRCh38
NC_000017.9:g.31231920G>T NCBI36
NG_015990.1:g.4571C>A

Transcript Alleles

HGVS Amino-acid Change
XR_934696.1:n.197-3579G>T
XR_934697.1:n.200-3579G>T
XR_001752852.1:n.426+729G>T
XR_934696.2:n.91-3579G>T
XR_934697.2:n.91-3579G>T