Canonical Allele Identifier: CA2726677877
Gene:

Linked Data

dbSNP Id: rs2137045044

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069312A>G , CM000674.2:g.80069312A>G GRCh38
NC_000012.11:g.80463092A>G , CM000674.1:g.80463092A>G GRCh37
NC_000012.10:g.78987223A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8130A>G
XR_945141.1:n.1758+8130A>G