Canonical Allele Identifier: CA3716464

Gene: PRRC2A

Linked Data

• ClinVar Variation Id: 2656407
• ClinVar RCV Id: RCV003431752 ; RCV003929152
• dbSNP Id: rs139053368
• ExAC: 6:31603046 C / T
• gnomAD v2: 6-31603046-C-T
• gnomAD v3: 6-31635269-C-T
• gnomAD v4: 6-31635269-C-T
• MyVariant Identifiers: chr6:g.31603046C>T (hg19) ; chr6:g.31635269C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635269C>T , CM000668.2:g.31635269C>T	GRCh38
NC_000006.11:g.31603046C>T , CM000668.1:g.31603046C>T	GRCh37
NC_000006.10:g.31711025C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5298C>T MANE Select	ENSP00000365201.2:p.Asp1766=
ENST00000376007.8:c.5298C>T	ENSP00000365175.4:p.Asp1766=
ENST00000376033.2:c.5298C>T	ENSP00000365201.2:p.Asp1766=
ENST00000469501.1:n.28C>T
ENST00000484787.1:n.709C>T
NM_004638.3:c.5298C>T	NP_004629.3:p.Asp1766=
NM_080686.2:c.5298C>T	NP_542417.2:p.Asp1766=
XM_011514890.1:c.5298C>T	XP_011513192.1:p.Asp1766=
XM_017011274.1:c.5298C>T	XP_016866763.1:p.Asp1766=
NM_004638.4:c.5298C>T MANE Select	NP_004629.3:p.Asp1766=
NM_080686.3:c.5298C>T	NP_542417.2:p.Asp1766=