Canonical Allele Identifier: CA3716456

Gene: PRRC2A

Linked Data

• dbSNP Id: rs764176032
• ExAC: 6:31603014 C / A
• gnomAD v2: 6-31603014-C-A
• gnomAD v4: 6-31635237-C-A
• MyVariant Identifiers: chr6:g.31603014C>A (hg19) ; chr6:g.31635237C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635237C>A , CM000668.2:g.31635237C>A	GRCh38
NC_000006.11:g.31603014C>A , CM000668.1:g.31603014C>A	GRCh37
NC_000006.10:g.31710993C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5266C>A MANE Select	ENSP00000365201.2:p.Pro1756Thr
ENST00000376007.8:c.5266C>A	ENSP00000365175.4:p.Pro1756Thr
ENST00000376033.2:c.5266C>A	ENSP00000365201.2:p.Pro1756Thr
ENST00000484787.1:n.677C>A
NM_004638.3:c.5266C>A	NP_004629.3:p.Pro1756Thr
NM_080686.2:c.5266C>A	NP_542417.2:p.Pro1756Thr
XM_011514890.1:c.5266C>A	XP_011513192.1:p.Pro1756Thr
XM_017011274.1:c.5266C>A	XP_016866763.1:p.Pro1756Thr
NM_004638.4:c.5266C>A MANE Select	NP_004629.3:p.Pro1756Thr
NM_080686.3:c.5266C>A	NP_542417.2:p.Pro1756Thr