Canonical Allele Identifier: CA2259611398

Gene: CCR7

Linked Data

• dbSNP Id: rs2036656772

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40561618A>C , CM000679.2:g.40561618A>C	GRCh38
NC_000017.10:g.38717870A>C , CM000679.1:g.38717870A>C	GRCh37
NC_000017.9:g.35971396A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246657.2:c.11-2676T>G MANE Select	ENSP00000246657.2:n.11-2676T>G
ENST00000578085.1:c.-130+3782T>G	ENSP00000463075.1:n.-130+3782T>G
NM_001301714.1:c.-130+3782T>G	NP_001288643.1:n.-130+3782T>G
NM_001838.3:c.11-2676T>G	NP_001829.1:n.11-2676T>G
NM_001838.4:c.11-2676T>G MANE Select	NP_001829.1:n.11-2676T>G
NM_001301714.2:c.-130+3782T>G	NP_001288643.1:n.-130+3782T>G