Canonical Allele Identifier: CA1605795077
Gene:

Linked Data

dbSNP Id: rs1761318984

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535838_1535841del , CM000668.2:g.1535838_1535841del GRCh38
NC_000006.11:g.1536073_1536076del , CM000668.1:g.1536073_1536076del GRCh37
NC_000006.10:g.1481072_1481075del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16508_234+16511del
XR_926380.1:n.218-2618_218-2615del
XR_926381.1:n.1108-2618_1108-2615del
XR_926382.1:n.235-6659_235-6656del
XR_926384.1:n.200-6659_200-6656del
XR_001743921.1:n.235-6683_235-6680del
XR_427861.3:n.234+16508_234+16511del
XR_926381.2:n.1123-2618_1123-2615del