Canonical Allele Identifier: CA916368046
Gene:

Linked Data

dbSNP Id: rs1557907859

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800601dup , CM000663.2:g.192800601dup GRCh38
NC_000001.10:g.192769731dup , CM000663.1:g.192769731dup GRCh37
NC_000001.9:g.191036354dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.31dup