Canonical Allele Identifier: CA449796791

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1330738760
• gnomAD v2: 6-31602944-C-T
• MyVariant Identifiers: chr6:g.31602944C>T (hg19) ; chr6:g.31635167C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635167C>T , CM000668.2:g.31635167C>T	GRCh38
NC_000006.11:g.31602944C>T , CM000668.1:g.31602944C>T	GRCh37
NC_000006.10:g.31710923C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5196C>T MANE Select	ENSP00000365201.2:p.Pro1732=
ENST00000376007.8:c.5196C>T	ENSP00000365175.4:p.Pro1732=
ENST00000376033.2:c.5196C>T	ENSP00000365201.2:p.Pro1732=
ENST00000484787.1:n.607C>T
NM_004638.3:c.5196C>T	NP_004629.3:p.Pro1732=
NM_080686.2:c.5196C>T	NP_542417.2:p.Pro1732=
XM_011514890.1:c.5196C>T	XP_011513192.1:p.Pro1732=
XM_017011274.1:c.5196C>T	XP_016866763.1:p.Pro1732=
NM_004638.4:c.5196C>T MANE Select	NP_004629.3:p.Pro1732=
NM_080686.3:c.5196C>T	NP_542417.2:p.Pro1732=