Canonical Allele Identifier: CA2637311308
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880798A>G , CM000679.2:g.35880798A>G GRCh38
NC_000017.9:g.31231915A>G NCBI36
NG_015990.1:g.4576T>C

Transcript Alleles

HGVS Amino-acid change
XR_934696.1:n.197-3584A>G
XR_934697.1:n.200-3584A>G
XR_001752852.1:n.426+724A>G
XR_934696.2:n.91-3584A>G
XR_934697.2:n.91-3584A>G