Canonical Allele Identifier: CA449661967
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1775446944
MyVariant Identifiers: chr6:g.31590614G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622837G>A , CM000668.2:g.31622837G>A GRCh38
NC_000006.11:g.31590614G>A , CM000668.1:g.31590614G>A GRCh37
NC_000006.10:g.31698593G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706625.1:c.64G>A ENSP00000516471.1:p.Val22Ile
ENST00000376033.3:c.48G>A MANE Select ENSP00000365201.2:p.Lys16=
ENST00000376007.8:c.48G>A ENSP00000365175.4:p.Lys16=
ENST00000376033.2:c.48G>A ENSP00000365201.2:p.Lys16=
ENST00000469577.5:n.136-1424G>A
NM_004638.3:c.48G>A NP_004629.3:p.Lys16=
NM_080686.2:c.48G>A NP_542417.2:p.Lys16=
XM_011514890.1:c.48G>A XP_011513192.1:p.Lys16=
XM_017011274.1:c.48G>A XP_016866763.1:p.Lys16=
NM_004638.4:c.48G>A MANE Select NP_004629.3:p.Lys16=
NM_080686.3:c.48G>A NP_542417.2:p.Lys16=
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