Canonical Allele Identifier: CA136867807
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs2844491

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000376033.3:c.5231G>C MANE Select ENSP00000365201.2:p.Gly1744Ala
ENST00000376007.8:c.5231G>C ENSP00000365175.4:p.Gly1744Ala
ENST00000376033.2:c.5231G>C ENSP00000365201.2:p.Gly1744Ala
ENST00000484787.1:n.642G>C
NM_004638.3:c.5231G>C NP_004629.3:p.Gly1744Ala
NM_080686.2:c.5231G>C NP_542417.2:p.Gly1744Ala
XM_011514890.1:c.5231G>C XP_011513192.1:p.Gly1744Ala
XM_017011274.1:c.5231G>C XP_016866763.1:p.Gly1744Ala
NM_004638.4:c.5231G>C MANE Select NP_004629.3:p.Gly1744Ala
NM_080686.3:c.5231G>C NP_542417.2:p.Gly1744Ala