Canonical Allele Identifier: CA2259611444
Gene: CCR7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40561738C= , CM000679.2:g.40561738C= GRCh38
NC_000017.10:g.38717990C= , CM000679.1:g.38717990C= GRCh37
NC_000017.9:g.35971516C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000246657.2:c.11-2796G= MANE Select ENSP00000246657.2:n.11-2796G=
ENST00000578085.1:c.-130+3662G= ENSP00000463075.1:n.-130+3662G=
NM_001301714.1:c.-130+3662G= NP_001288643.1:n.-130+3662G=
NM_001838.3:c.11-2796G= NP_001829.1:n.11-2796G=
NM_001838.4:c.11-2796G= MANE Select NP_001829.1:n.11-2796G=
NM_001301714.2:c.-130+3662G= NP_001288643.1:n.-130+3662G=
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