Canonical Allele Identifier: CA1619235160
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1775428247

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622706C>G , CM000668.2:g.31622706C>G GRCh38
NC_000006.11:g.31590483C>G , CM000668.1:g.31590483C>G GRCh37
NC_000006.10:g.31698462C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-84C>G MANE Select ENSP00000365201.2:n.-84C>G
ENST00000376007.8:c.-63-21C>G ENSP00000365175.4:n.-63-21C>G
ENST00000376033.2:c.-84C>G ENSP00000365201.2:n.-84C>G
ENST00000469577.5:n.136-1555C>G
NM_004638.3:c.-84C>G NP_004629.3:n.-84C>G
NM_080686.2:c.-63-21C>G NP_542417.2:n.-63-21C>G
XM_011514890.1:c.-63-21C>G XP_011513192.1:n.-63-21C>G
NM_004638.4:c.-84C>G MANE Select NP_004629.3:n.-84C>G
NM_080686.3:c.-63-21C>G NP_542417.2:n.-63-21C>G