Canonical Allele Identifier: CA983684447
Gene: CCR7 HGNC NCBI

Linked Data

dbSNP Id: rs2036656876
gnomAD v3: 17-40561634-G-A
gnomAD v4: 17-40561634-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40561634G>A , CM000679.2:g.40561634G>A GRCh38
NC_000017.10:g.38717886G>A , CM000679.1:g.38717886G>A GRCh37
NC_000017.9:g.35971412G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000246657.2:c.11-2692C>T MANE Select ENSP00000246657.2:n.11-2692C>T
ENST00000578085.1:c.-130+3766C>T ENSP00000463075.1:n.-130+3766C>T
NM_001301714.1:c.-130+3766C>T NP_001288643.1:n.-130+3766C>T
NM_001838.3:c.11-2692C>T NP_001829.1:n.11-2692C>T
NM_001838.4:c.11-2692C>T MANE Select NP_001829.1:n.11-2692C>T
NM_001301714.2:c.-130+3766C>T NP_001288643.1:n.-130+3766C>T
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