Canonical Allele Identifier: CA449661996
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31622897-C-A
MyVariant Identifiers: chr6:g.31590674C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622897C>A , CM000668.2:g.31622897C>A GRCh38
NC_000006.11:g.31590674C>A , CM000668.1:g.31590674C>A GRCh37
NC_000006.10:g.31698653C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.108C>A MANE Select ENSP00000365201.2:p.Pro36=
ENST00000376007.8:c.108C>A ENSP00000365175.4:p.Pro36=
ENST00000376033.2:c.108C>A ENSP00000365201.2:p.Pro36=
ENST00000469577.5:n.136-1364C>A
NM_004638.3:c.108C>A NP_004629.3:p.Pro36=
NM_080686.2:c.108C>A NP_542417.2:p.Pro36=
XM_011514890.1:c.108C>A XP_011513192.1:p.Pro36=
XM_017011274.1:c.108C>A XP_016866763.1:p.Pro36=
NM_004638.4:c.108C>A MANE Select NP_004629.3:p.Pro36=
NM_080686.3:c.108C>A NP_542417.2:p.Pro36=
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