Canonical Allele Identifier: CA528081325
Gene:

Linked Data

dbSNP Id: rs77847085

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800600dup , CM000663.2:g.192800600dup GRCh38
NC_000001.10:g.192769730dup , CM000663.1:g.192769730dup GRCh37
NC_000001.9:g.191036353dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.30dup