Canonical Allele Identifier: CA983684456
Gene: CCR7 HGNC NCBI

Linked Data

dbSNP Id: rs2036657111

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40561646T>A , CM000679.2:g.40561646T>A GRCh38
NC_000017.10:g.38717898T>A , CM000679.1:g.38717898T>A GRCh37
NC_000017.9:g.35971424T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000246657.2:c.11-2704A>T MANE Select ENSP00000246657.2:n.11-2704A>T
ENST00000578085.1:c.-130+3754A>T ENSP00000463075.1:n.-130+3754A>T
NM_001301714.1:c.-130+3754A>T NP_001288643.1:n.-130+3754A>T
NM_001838.3:c.11-2704A>T NP_001829.1:n.11-2704A>T
NM_001838.4:c.11-2704A>T MANE Select NP_001829.1:n.11-2704A>T
NM_001301714.2:c.-130+3754A>T NP_001288643.1:n.-130+3754A>T