Canonical Allele Identifier: CA3716403
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs781034986
ExAC: 6:31602668 C / A
gnomAD v2: 6-31602668-C-A
gnomAD v3: 6-31634891-C-A
gnomAD v4: 6-31634891-C-A
MyVariant Identifiers: chr6:g.31602668C>A (hg19) chr6:g.31634891C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31634891C>A , CM000668.2:g.31634891C>A GRCh38
NC_000006.11:g.31602668C>A , CM000668.1:g.31602668C>A GRCh37
NC_000006.10:g.31710647C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5074C>A MANE Select ENSP00000365201.2:p.Pro1692Thr
ENST00000376007.8:c.5074C>A ENSP00000365175.4:p.Pro1692Thr
ENST00000376033.2:c.5074C>A ENSP00000365201.2:p.Pro1692Thr
ENST00000484787.1:n.485C>A
NM_004638.3:c.5074C>A NP_004629.3:p.Pro1692Thr
NM_080686.2:c.5074C>A NP_542417.2:p.Pro1692Thr
XM_011514890.1:c.5074C>A XP_011513192.1:p.Pro1692Thr
XM_017011274.1:c.5074C>A XP_016866763.1:p.Pro1692Thr
NM_004638.4:c.5074C>A MANE Select NP_004629.3:p.Pro1692Thr
NM_080686.3:c.5074C>A NP_542417.2:p.Pro1692Thr
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