Canonical Allele Identifier: CA309668943

Gene:

Linked Data

• dbSNP Id: rs386810270

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50837538_50837539delinsAA , CM000681.2:g.50837538_50837539delinsAA	GRCh38
NC_000019.9:g.51340794_51340795delinsAA , CM000681.1:g.51340794_51340795delinsAA	GRCh37
NC_000019.8:g.56032606_56032607delinsAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_131203.1:n.213+6245_213+6246delinsAA
NR_131205.1:n.230+6245_230+6246delinsAA
XR_936030.1:n.298+6245_298+6246delinsAA
XR_936031.1:n.298+6245_298+6246delinsAA
XR_936032.1:n.298+6245_298+6246delinsAA
XR_936033.1:n.294+6245_294+6246delinsAA
XR_936035.1:n.281+6245_281+6246delinsAA