Canonical Allele Identifier: CA2677997048
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31622728-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622728C>G , CM000668.2:g.31622728C>G GRCh38
NC_000006.11:g.31590505C>G , CM000668.1:g.31590505C>G GRCh37
NC_000006.10:g.31698484C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-62C>G MANE Select ENSP00000365201.2:n.-62C>G
ENST00000376007.8:c.-62C>G ENSP00000365175.4:n.-62C>G
ENST00000376033.2:c.-62C>G ENSP00000365201.2:n.-62C>G
ENST00000469577.5:n.136-1533C>G
NM_004638.3:c.-62C>G NP_004629.3:n.-62C>G
NM_080686.2:c.-62C>G NP_542417.2:n.-62C>G
XM_011514890.1:c.-62C>G XP_011513192.1:n.-62C>G
NM_004638.4:c.-62C>G MANE Select NP_004629.3:n.-62C>G
NM_080686.3:c.-62C>G NP_542417.2:n.-62C>G