Canonical Allele Identifier: CA290547161

Gene: CCR7

Linked Data

• dbSNP Id: rs764114141
• gnomAD v2: 17-38717810-A-T
• gnomAD v3: 17-40561558-A-T
• gnomAD v4: 17-40561558-A-T
• MyVariant Identifiers: chr17:g.38717810A>T (hg19) ; chr17:g.40561558A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40561558A>T , CM000679.2:g.40561558A>T	GRCh38
NC_000017.10:g.38717810A>T , CM000679.1:g.38717810A>T	GRCh37
NC_000017.9:g.35971336A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246657.2:c.11-2616T>A MANE Select	ENSP00000246657.2:n.11-2616T>A
ENST00000578085.1:c.-130+3842T>A	ENSP00000463075.1:n.-130+3842T>A
NM_001301714.1:c.-130+3842T>A	NP_001288643.1:n.-130+3842T>A
NM_001838.3:c.11-2616T>A	NP_001829.1:n.11-2616T>A
NM_001838.4:c.11-2616T>A MANE Select	NP_001829.1:n.11-2616T>A
NM_001301714.2:c.-130+3842T>A	NP_001288643.1:n.-130+3842T>A