Canonical Allele Identifier: CA136852511
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs9688644
gnomAD v3: 6-31622891-G-A
gnomAD v4: 6-31622891-G-A
MyVariant Identifiers: chr6:g.31590668G>A (hg19) chr6:g.31622891G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622891G>A , CM000668.2:g.31622891G>A GRCh38
NC_000006.11:g.31590668G>A , CM000668.1:g.31590668G>A GRCh37
NC_000006.10:g.31698647G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.102G>A MANE Select ENSP00000365201.2:p.Gln34=
ENST00000376007.8:c.102G>A ENSP00000365175.4:p.Gln34=
ENST00000376033.2:c.102G>A ENSP00000365201.2:p.Gln34=
ENST00000469577.5:n.136-1370G>A
NM_004638.3:c.102G>A NP_004629.3:p.Gln34=
NM_080686.2:c.102G>A NP_542417.2:p.Gln34=
XM_011514890.1:c.102G>A XP_011513192.1:p.Gln34=
XM_017011274.1:c.102G>A XP_016866763.1:p.Gln34=
NM_004638.4:c.102G>A MANE Select NP_004629.3:p.Gln34=
NM_080686.3:c.102G>A NP_542417.2:p.Gln34=
Search 100 bp 5'
Search 100 bp 3'