Canonical Allele Identifier: CA363364758

Gene: PRRC2A

Linked Data

• dbSNP Id: rs2844491
• gnomAD v3: 6-31635202-G-T
• gnomAD v4: 6-31635202-G-T
• MyVariant Identifiers: chr6:g.31602979G>T (hg19) ; chr6:g.31635202G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635202G>T , CM000668.2:g.31635202G>T	GRCh38
NC_000006.11:g.31602979G>T , CM000668.1:g.31602979G>T	GRCh37
NC_000006.10:g.31710958G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376033.3:c.5231G>T MANE Select	ENSP00000365201.2:p.Gly1744Val
ENST00000376007.8:c.5231G>T	ENSP00000365175.4:p.Gly1744Val
ENST00000376033.2:c.5231G>T	ENSP00000365201.2:p.Gly1744Val
ENST00000484787.1:n.642G>T
NM_004638.3:c.5231G>T	NP_004629.3:p.Gly1744Val
NM_080686.2:c.5231G>T	NP_542417.2:p.Gly1744Val
XM_011514890.1:c.5231G>T	XP_011513192.1:p.Gly1744Val
XM_017011274.1:c.5231G>T	XP_016866763.1:p.Gly1744Val
NM_004638.4:c.5231G>T MANE Select	NP_004629.3:p.Gly1744Val
NM_080686.3:c.5231G>T	NP_542417.2:p.Gly1744Val