Canonical Allele Identifier: CA185773140

Gene: CASC11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127705823G>T , CM000670.2:g.127705823G>T	GRCh38
NC_000008.10:g.128718068G>T , CM000670.1:g.128718068G>T	GRCh37
NC_000008.9:g.128787250G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_117102.1:n.366-2580C>A