Canonical Allele Identifier: CA2578565729
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31622716-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622716C>A , CM000668.2:g.31622716C>A GRCh38
NC_000006.11:g.31590493C>A , CM000668.1:g.31590493C>A GRCh37
NC_000006.10:g.31698472C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-74C>A MANE Select ENSP00000365201.2:n.-74C>A
ENST00000376007.8:c.-63-11C>A ENSP00000365175.4:n.-63-11C>A
ENST00000376033.2:c.-74C>A ENSP00000365201.2:n.-74C>A
ENST00000469577.5:n.136-1545C>A
NM_004638.3:c.-74C>A NP_004629.3:n.-74C>A
NM_080686.2:c.-63-11C>A NP_542417.2:n.-63-11C>A
XM_011514890.1:c.-63-11C>A XP_011513192.1:n.-63-11C>A
NM_004638.4:c.-74C>A MANE Select NP_004629.3:n.-74C>A
NM_080686.3:c.-63-11C>A NP_542417.2:n.-63-11C>A
Search 100 bp 5'
Search 100 bp 3'