Canonical Allele Identifier: CA2716575553
Gene:

Linked Data

dbSNP Id: rs2129024380

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.9400145T>G , CM000670.2:g.9400145T>G GRCh38
NC_000008.10:g.9257655T>G , CM000670.1:g.9257655T>G GRCh37
NC_000008.9:g.9295065T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948936.1:n.185+3800A>C
XR_948940.1:n.96-3718T>G
XR_948941.1:n.96-13504T>G
XR_002956685.1:n.99-3718T>G
XR_948940.2:n.99-3718T>G
XR_948941.2:n.99-13504T>G