Canonical Allele Identifier: CA1157252084
Gene:

Linked Data

dbSNP Id: rs2045188722

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19874421_19874424del , CM000663.2:g.19874421_19874424del GRCh38
NC_000001.10:g.20200914_20200917del , CM000663.1:g.20200914_20200917del GRCh37
NC_000001.9:g.20073501_20073504del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947027.1:n.266-8665_266-8662del
XR_947028.1:n.266-8665_266-8662del
XR_947027.2:n.167-8665_167-8662del
XR_947028.2:n.167-8665_167-8662del