Canonical Allele Identifier: CA363363894

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1287269876
• gnomAD v2: 6-31602669-C-A
• gnomAD v4: 6-31634892-C-A
• MyVariant Identifiers: chr6:g.31602669C>A (hg19) ; chr6:g.31634892C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31634892C>A , CM000668.2:g.31634892C>A	GRCh38
NC_000006.11:g.31602669C>A , CM000668.1:g.31602669C>A	GRCh37
NC_000006.10:g.31710648C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5075C>A MANE Select	ENSP00000365201.2:p.Pro1692His
ENST00000376007.8:c.5075C>A	ENSP00000365175.4:p.Pro1692His
ENST00000376033.2:c.5075C>A	ENSP00000365201.2:p.Pro1692His
ENST00000484787.1:n.486C>A
NM_004638.3:c.5075C>A	NP_004629.3:p.Pro1692His
NM_080686.2:c.5075C>A	NP_542417.2:p.Pro1692His
XM_011514890.1:c.5075C>A	XP_011513192.1:p.Pro1692His
XM_017011274.1:c.5075C>A	XP_016866763.1:p.Pro1692His
NM_004638.4:c.5075C>A MANE Select	NP_004629.3:p.Pro1692His
NM_080686.3:c.5075C>A	NP_542417.2:p.Pro1692His