Canonical Allele Identifier: CA290547180

Gene: CCR7

Linked Data

• dbSNP Id: rs367822579
• gnomAD v2: 17-38717839-C-G
• gnomAD v3: 17-40561587-C-G
• gnomAD v4: 17-40561587-C-G
• MyVariant Identifiers: chr17:g.38717839C>G (hg19) ; chr17:g.40561587C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40561587C>G , CM000679.2:g.40561587C>G	GRCh38
NC_000017.10:g.38717839C>G , CM000679.1:g.38717839C>G	GRCh37
NC_000017.9:g.35971365C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246657.2:c.11-2645G>C MANE Select	ENSP00000246657.2:n.11-2645G>C
ENST00000578085.1:c.-130+3813G>C	ENSP00000463075.1:n.-130+3813G>C
NM_001301714.1:c.-130+3813G>C	NP_001288643.1:n.-130+3813G>C
NM_001838.3:c.11-2645G>C	NP_001829.1:n.11-2645G>C
NM_001838.4:c.11-2645G>C MANE Select	NP_001829.1:n.11-2645G>C
NM_001301714.2:c.-130+3813G>C	NP_001288643.1:n.-130+3813G>C