Canonical Allele Identifier: CA14378562

Gene: CCR7

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40563547C>T , CM000679.2:g.40563547C>T	GRCh38
NC_000017.10:g.38719799C>T , CM000679.1:g.38719799C>T	GRCh37
NC_000017.9:g.35973325C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246657.2:c.10+1853G>A MANE Select	ENSP00000246657.2:n.10+1853G>A
ENST00000578085.1:c.-130+1853G>A	ENSP00000463075.1:n.-130+1853G>A
NM_001301714.1:c.-130+1853G>A	NP_001288643.1:n.-130+1853G>A
NM_001838.3:c.10+1853G>A	NP_001829.1:n.10+1853G>A
NM_001838.4:c.10+1853G>A MANE Select	NP_001829.1:n.10+1853G>A
NM_001301714.2:c.-130+1853G>A	NP_001288643.1:n.-130+1853G>A