Canonical Allele Identifier: CA2259611452

Gene: CCR7

Linked Data

• dbSNP Id: rs1597725103

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40561752C>G , CM000679.2:g.40561752C>G	GRCh38
NC_000017.10:g.38718004C>G , CM000679.1:g.38718004C>G	GRCh37
NC_000017.9:g.35971530C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246657.2:c.11-2810G>C MANE Select	ENSP00000246657.2:n.11-2810G>C
ENST00000578085.1:c.-130+3648G>C	ENSP00000463075.1:n.-130+3648G>C
NM_001301714.1:c.-130+3648G>C	NP_001288643.1:n.-130+3648G>C
NM_001838.3:c.11-2810G>C	NP_001829.1:n.11-2810G>C
NM_001838.4:c.11-2810G>C MANE Select	NP_001829.1:n.11-2810G>C
NM_001301714.2:c.-130+3648G>C	NP_001288643.1:n.-130+3648G>C