Canonical Allele Identifier: CA936775912
Gene:

Linked Data

dbSNP Id: rs1851778329

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812733_34812734del , CM000673.2:g.34812733_34812734del GRCh38
NC_000011.9:g.34834280_34834281del , CM000673.1:g.34834280_34834281del GRCh37
NC_000011.8:g.34790856_34790857del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+58126_579+58127del
XR_931188.1:n.693+58126_693+58127del
XR_931189.1:n.854+58126_854+58127del
XR_931190.1:n.639+58126_639+58127del
XR_931191.1:n.689+58126_689+58127del
XR_001748174.1:n.855+58126_855+58127del
XR_001748176.1:n.1016+58126_1016+58127del
XR_002957246.1:n.639+58126_639+58127del