Canonical Allele Identifier: CA625973854
Gene: CCR7 HGNC NCBI

Linked Data

dbSNP Id: rs1433325444
gnomAD v2: 17-38717935-TCCTCCAGACTG-T
gnomAD v3: 17-40561683-TCCTCCAGACTG-T
gnomAD v4: 17-40561683-TCCTCCAGACTG-T
MyVariant Identifiers: chr17:g.38717936_38717946del (hg19) chr17:g.40561684_40561694del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40561686_40561696del , CM000679.2:g.40561686_40561696del GRCh38
NC_000017.10:g.38717938_38717948del , CM000679.1:g.38717938_38717948del GRCh37
NC_000017.9:g.35971464_35971474del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000246657.2:c.11-2752_11-2742del MANE Select ENSP00000246657.2:n.11-2752_11-2742del
ENST00000578085.1:c.-130+3706_-130+3716del ENSP00000463075.1:n.-130+3706_-130+3716de...
NM_001301714.1:c.-130+3706_-130+3716del NP_001288643.1:n.-130+3706_-130+3716del
NM_001838.3:c.11-2752_11-2742del NP_001829.1:n.11-2752_11-2742del
NM_001838.4:c.11-2752_11-2742del MANE Select NP_001829.1:n.11-2752_11-2742del
NM_001301714.2:c.-130+3706_-130+3716del NP_001288643.1:n.-130+3706_-130+3716del
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