Canonical Allele Identifier: CA2809469768

Gene: CCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40561625T>C , CM000679.2:g.40561625T>C	GRCh38
NC_000017.10:g.38717877T>C , CM000679.1:g.38717877T>C	GRCh37
NC_000017.9:g.35971403T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246657.2:c.11-2683A>G MANE Select	ENSP00000246657.2:n.11-2683A>G
ENST00000578085.1:c.-130+3775A>G	ENSP00000463075.1:n.-130+3775A>G
NM_001301714.1:c.-130+3775A>G	NP_001288643.1:n.-130+3775A>G
NM_001838.3:c.11-2683A>G	NP_001829.1:n.11-2683A>G
NM_001838.4:c.11-2683A>G MANE Select	NP_001829.1:n.11-2683A>G
NM_001301714.2:c.-130+3775A>G	NP_001288643.1:n.-130+3775A>G