Canonical Allele Identifier: CA449796806
Gene: PRRC2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31602953A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635176A>T , CM000668.2:g.31635176A>T GRCh38
NC_000006.11:g.31602953A>T , CM000668.1:g.31602953A>T GRCh37
NC_000006.10:g.31710932A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5205A>T MANE Select ENSP00000365201.2:p.Thr1735=
ENST00000376007.8:c.5205A>T ENSP00000365175.4:p.Thr1735=
ENST00000376033.2:c.5205A>T ENSP00000365201.2:p.Thr1735=
ENST00000484787.1:n.616A>T
NM_004638.3:c.5205A>T NP_004629.3:p.Thr1735=
NM_080686.2:c.5205A>T NP_542417.2:p.Thr1735=
XM_011514890.1:c.5205A>T XP_011513192.1:p.Thr1735=
XM_017011274.1:c.5205A>T XP_016866763.1:p.Thr1735=
NM_004638.4:c.5205A>T MANE Select NP_004629.3:p.Thr1735=
NM_080686.3:c.5205A>T NP_542417.2:p.Thr1735=