Canonical Allele Identifier: CA1619157176
Gene:

Linked Data

dbSNP Id: rs1761792852

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440058del , CM000668.2:g.31440058del GRCh38
NC_000006.11:g.31407835del , CM000668.1:g.31407835del GRCh37
NC_000006.10:g.31515814del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-4del