Canonical Allele Identifier: CA220638150
Gene:

Linked Data

dbSNP Id: rs934115515

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759301T>G , CM000673.2:g.34759301T>G GRCh38
NC_000011.9:g.34780848T>G , CM000673.1:g.34780848T>G GRCh37
NC_000011.8:g.34737424T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+4694T>G
XR_931188.1:n.693+4694T>G
XR_931189.1:n.854+4694T>G
XR_931190.1:n.639+4694T>G
XR_931191.1:n.689+4694T>G
XR_001748174.1:n.855+4694T>G
XR_001748176.1:n.1016+4694T>G
XR_002957246.1:n.639+4694T>G