Canonical Allele Identifier: CA363364607
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1395769051
gnomAD v2: 6-31602939-G-T
gnomAD v4: 6-31635162-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635162G>T , CM000668.2:g.31635162G>T GRCh38
NC_000006.11:g.31602939G>T , CM000668.1:g.31602939G>T GRCh37
NC_000006.10:g.31710918G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5191G>T MANE Select ENSP00000365201.2:p.Gly1731Cys
ENST00000376007.8:c.5191G>T ENSP00000365175.4:p.Gly1731Cys
ENST00000376033.2:c.5191G>T ENSP00000365201.2:p.Gly1731Cys
ENST00000484787.1:n.602G>T
NM_004638.3:c.5191G>T NP_004629.3:p.Gly1731Cys
NM_080686.2:c.5191G>T NP_542417.2:p.Gly1731Cys
XM_011514890.1:c.5191G>T XP_011513192.1:p.Gly1731Cys
XM_017011274.1:c.5191G>T XP_016866763.1:p.Gly1731Cys
NM_004638.4:c.5191G>T MANE Select NP_004629.3:p.Gly1731Cys
NM_080686.3:c.5191G>T NP_542417.2:p.Gly1731Cys