Canonical Allele Identifier: CA2049072535
Gene:

Linked Data

dbSNP Id: rs1458309370

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069329C>G , CM000674.2:g.80069329C>G GRCh38
NC_000012.11:g.80463109C>G , CM000674.1:g.80463109C>G GRCh37
NC_000012.10:g.78987240C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8147C>G
XR_945141.1:n.1758+8147C>G