Canonical Allele Identifier: CA2269950705
Gene:

Linked Data

dbSNP Id: rs2030907403

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498408_63498422del , CM000679.2:g.63498408_63498422del GRCh38
NC_000017.10:g.61575769_61575783del , CM000679.1:g.61575769_61575783del GRCh37
NC_000017.9:g.58929501_58929515del NCBI36
NG_011648.1:g.26336_26350del

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1969+1423_1969+1437del ENSP00000464149.1:n.1969+1423_1969+1437del