Canonical Allele Identifier: CA206723624
Gene:

Linked Data

dbSNP Id: rs1039290044

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318623A>G , CM000672.2:g.43318623A>G GRCh38
NC_000010.10:g.43814071A>G , CM000672.1:g.43814071A>G GRCh37
NC_000010.9:g.43134077A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+28A>G
XR_945902.2:n.198+28A>G