Canonical Allele Identifier: CA449797119

Gene: PRRC2A

Linked Data

• dbSNP Id: rs2150532970
• MyVariant Identifiers: chr6:g.31602917C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635140C>G , CM000668.2:g.31635140C>G	GRCh38
NC_000006.11:g.31602917C>G , CM000668.1:g.31602917C>G	GRCh37
NC_000006.10:g.31710896C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5169C>G MANE Select	ENSP00000365201.2:p.Pro1723=
ENST00000376007.8:c.5169C>G	ENSP00000365175.4:p.Pro1723=
ENST00000376033.2:c.5169C>G	ENSP00000365201.2:p.Pro1723=
ENST00000484787.1:n.580C>G
NM_004638.3:c.5169C>G	NP_004629.3:p.Pro1723=
NM_080686.2:c.5169C>G	NP_542417.2:p.Pro1723=
XM_011514890.1:c.5169C>G	XP_011513192.1:p.Pro1723=
XM_017011274.1:c.5169C>G	XP_016866763.1:p.Pro1723=
NM_004638.4:c.5169C>G MANE Select	NP_004629.3:p.Pro1723=
NM_080686.3:c.5169C>G	NP_542417.2:p.Pro1723=