Canonical Allele Identifier: CA449796954
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31634920-A-C
MyVariant Identifiers: chr6:g.31602697A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31634920A>C , CM000668.2:g.31634920A>C GRCh38
NC_000006.11:g.31602697A>C , CM000668.1:g.31602697A>C GRCh37
NC_000006.10:g.31710676A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5103A>C MANE Select ENSP00000365201.2:p.Pro1701=
ENST00000376007.8:c.5103A>C ENSP00000365175.4:p.Pro1701=
ENST00000376033.2:c.5103A>C ENSP00000365201.2:p.Pro1701=
ENST00000484787.1:n.514A>C
NM_004638.3:c.5103A>C NP_004629.3:p.Pro1701=
NM_080686.2:c.5103A>C NP_542417.2:p.Pro1701=
XM_011514890.1:c.5103A>C XP_011513192.1:p.Pro1701=
XM_017011274.1:c.5103A>C XP_016866763.1:p.Pro1701=
NM_004638.4:c.5103A>C MANE Select NP_004629.3:p.Pro1701=
NM_080686.3:c.5103A>C NP_542417.2:p.Pro1701=
Search 100 bp 5'
Search 100 bp 3'