Canonical Allele Identifier: CA454704111
Community Standard Title: NC_000007.14:g.38349487C>G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.38349487C>G , CM000669.2:g.38349487C>G GRCh38
NC_000007.13:g.38389088C>G , CM000669.1:g.38389088C>G GRCh37
NC_000007.12:g.38355613C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040085.1:n.331-859C>G (TRG-AS1)
ENST00000390344.2:c.222G>C (TRGV5) ENSP00000374867.2:p.Lys74Asn
ENST00000610547.1:c.380+18065G>C (TRGC2) ENSP00000480566.1:n.380+18065G>C
ENST00000613175.1:c.222G>C (TRGV5) ENSP00000483079.1:p.Lys74Asn