Canonical Allele Identifier: CA2711422078

Gene: PRRC2A

Linked Data

• dbSNP Id: rs2150489952

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622659A>G , CM000668.2:g.31622659A>G	GRCh38
NC_000006.11:g.31590436A>G , CM000668.1:g.31590436A>G	GRCh37
NC_000006.10:g.31698415A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.-100-31A>G MANE Select	ENSP00000365201.2:n.-100-31A>G
ENST00000376007.8:c.-63-68A>G	ENSP00000365175.4:n.-63-68A>G
ENST00000376033.2:c.-100-31A>G	ENSP00000365201.2:n.-100-31A>G
ENST00000469577.5:n.136-1602A>G
NM_004638.3:c.-100-31A>G	NP_004629.3:n.-100-31A>G
NM_080686.2:c.-63-68A>G	NP_542417.2:n.-63-68A>G
XM_011514890.1:c.-63-68A>G	XP_011513192.1:n.-63-68A>G
NM_004638.4:c.-100-31A>G MANE Select	NP_004629.3:n.-100-31A>G
NM_080686.3:c.-63-68A>G	NP_542417.2:n.-63-68A>G