Canonical Allele Identifier: CA433592645
Gene: CCR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.46399210C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46357719C>T , CM000665.2:g.46357719C>T GRCh38
NC_000003.11:g.46399210C>T , CM000665.1:g.46399210C>T GRCh37
NC_000003.10:g.46374214C>T NCBI36
NG_021428.1:g.8976C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000445132.3:c.192C>T MANE Select ENSP00000399285.2:p.Val64=
ENST00000292301.4:c.192C>T ENSP00000292301.3:p.Val64=
ENST00000400888.2:c.192C>T ENSP00000383681.2:p.Val64=
ENST00000421659.1:c.192C>T ENSP00000396736.1:p.Val64=
ENST00000445132.2:c.192C>T ENSP00000399285.2:p.Val64=
ENST00000465202.1:n.315-398C>T
NM_001123041.2:c.192C>T NP_001116513.2:p.Val64=
NM_001123396.1:c.192C>T NP_001116868.1:p.Val64=
XM_011534069.1:c.192C>T XP_011532371.1:p.Val64=
NM_001123396.2:c.192C>T NP_001116868.1:p.Val64=
NM_001123396.3:c.192C>T NP_001116868.1:p.Val64=
NM_001123041.3:c.192C>T NP_001116513.2:p.Val64=
NM_001123396.4:c.192C>T MANE Select NP_001116868.1:p.Val64=