Canonical Allele Identifier: CA363364129
Gene: PRRC2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31602702G>A (hg19) chr6:g.31634925G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31634925G>A , CM000668.2:g.31634925G>A GRCh38
NC_000006.11:g.31602702G>A , CM000668.1:g.31602702G>A GRCh37
NC_000006.10:g.31710681G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5108G>A MANE Select ENSP00000365201.2:p.Gly1703Asp
ENST00000376007.8:c.5108G>A ENSP00000365175.4:p.Gly1703Asp
ENST00000376033.2:c.5108G>A ENSP00000365201.2:p.Gly1703Asp
ENST00000484787.1:n.519G>A
NM_004638.3:c.5108G>A NP_004629.3:p.Gly1703Asp
NM_080686.2:c.5108G>A NP_542417.2:p.Gly1703Asp
XM_011514890.1:c.5108G>A XP_011513192.1:p.Gly1703Asp
XM_017011274.1:c.5108G>A XP_016866763.1:p.Gly1703Asp
NM_004638.4:c.5108G>A MANE Select NP_004629.3:p.Gly1703Asp
NM_080686.3:c.5108G>A NP_542417.2:p.Gly1703Asp
Search 100 bp 5'
Search 100 bp 3'