Canonical Allele Identifier: CA1619235201
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1775432796

Genomic Alleles

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

Transcript Alleles

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