Canonical Allele Identifier: CA1007769621
Gene:

Linked Data

dbSNP Id: rs1653212773

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152328367_152328378del , CM000663.2:g.152328367_152328378del GRCh38
NC_000001.10:g.152300843_152300854del , CM000663.1:g.152300843_152300854del GRCh37
NC_000001.9:g.150567467_150567478del NCBI36
NG_016190.1:g.1828_1839del , LRG_1028:g.1828_1839del

Transcript Alleles

HGVS Amino-acid Change
NR_103778.1:n.915-4216_915-4205del