Canonical Allele Identifier: CA771954288
Gene: CCR7 HGNC NCBI

Linked Data

dbSNP Id: rs1211277491
MyVariant Identifiers: chr17:g.38717705G>C (hg19) chr17:g.40561453G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40561453G>C , CM000679.2:g.40561453G>C GRCh38
NC_000017.10:g.38717705G>C , CM000679.1:g.38717705G>C GRCh37
NC_000017.9:g.35971231G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000246657.2:c.11-2511C>G MANE Select ENSP00000246657.2:n.11-2511C>G
ENST00000578085.1:c.-130+3947C>G ENSP00000463075.1:n.-130+3947C>G
NM_001301714.1:c.-130+3947C>G NP_001288643.1:n.-130+3947C>G
NM_001838.3:c.11-2511C>G NP_001829.1:n.11-2511C>G
NM_001838.4:c.11-2511C>G MANE Select NP_001829.1:n.11-2511C>G
NM_001301714.2:c.-130+3947C>G NP_001288643.1:n.-130+3947C>G
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