Canonical Allele Identifier: CA136867689
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1022862519
gnomAD v4: 6-31635102-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635102C>G , CM000668.2:g.31635102C>G GRCh38
NC_000006.11:g.31602879C>G , CM000668.1:g.31602879C>G GRCh37
NC_000006.10:g.31710858C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376033.3:c.5161-30C>G MANE Select ENSP00000365201.2:n.5161-30C>G
ENST00000376007.8:c.5161-30C>G ENSP00000365175.4:n.5161-30C>G
ENST00000376033.2:c.5161-30C>G ENSP00000365201.2:n.5161-30C>G
ENST00000484787.1:n.572-30C>G
NM_004638.3:c.5161-30C>G NP_004629.3:n.5161-30C>G
NM_080686.2:c.5161-30C>G NP_542417.2:n.5161-30C>G
XM_011514890.1:c.5161-30C>G XP_011513192.1:n.5161-30C>G
XM_017011274.1:c.5161-30C>G XP_016866763.1:n.5161-30C>G
NM_004638.4:c.5161-30C>G MANE Select NP_004629.3:n.5161-30C>G
NM_080686.3:c.5161-30C>G NP_542417.2:n.5161-30C>G