Canonical Allele Identifier: CA625973853
Gene: CCR7 HGNC NCBI

Linked Data

dbSNP Id: rs1424005092
gnomAD v2: 17-38717922-A-T
gnomAD v3: 17-40561670-A-T
gnomAD v4: 17-40561670-A-T
MyVariant Identifiers: chr17:g.38717922A>T (hg19) chr17:g.40561670A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40561670A>T , CM000679.2:g.40561670A>T GRCh38
NC_000017.10:g.38717922A>T , CM000679.1:g.38717922A>T GRCh37
NC_000017.9:g.35971448A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000246657.2:c.11-2728T>A MANE Select ENSP00000246657.2:n.11-2728T>A
ENST00000578085.1:c.-130+3730T>A ENSP00000463075.1:n.-130+3730T>A
NM_001301714.1:c.-130+3730T>A NP_001288643.1:n.-130+3730T>A
NM_001838.3:c.11-2728T>A NP_001829.1:n.11-2728T>A
NM_001838.4:c.11-2728T>A MANE Select NP_001829.1:n.11-2728T>A
NM_001301714.2:c.-130+3730T>A NP_001288643.1:n.-130+3730T>A
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