Canonical Allele Identifier: CA1963375939
Gene:

Linked Data

dbSNP Id: rs1590627787

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759335C>T , CM000673.2:g.34759335C>T GRCh38
NC_000011.9:g.34780882C>T , CM000673.1:g.34780882C>T GRCh37
NC_000011.8:g.34737458C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+4728C>T
XR_931188.1:n.693+4728C>T
XR_931189.1:n.854+4728C>T
XR_931190.1:n.639+4728C>T
XR_931191.1:n.689+4728C>T
XR_001748174.1:n.855+4728C>T
XR_001748176.1:n.1016+4728C>T
XR_002957246.1:n.639+4728C>T