Canonical Allele Identifier: CA1619240488
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1777148949
gnomAD v4: 6-31634994-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31634994G>A , CM000668.2:g.31634994G>A GRCh38
NC_000006.11:g.31602771G>A , CM000668.1:g.31602771G>A GRCh37
NC_000006.10:g.31710750G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5160+17G>A MANE Select ENSP00000365201.2:n.5160+17G>A
ENST00000376007.8:c.5160+17G>A ENSP00000365175.4:n.5160+17G>A
ENST00000376033.2:c.5160+17G>A ENSP00000365201.2:n.5160+17G>A
ENST00000484787.1:n.571+17G>A
NM_004638.3:c.5160+17G>A NP_004629.3:n.5160+17G>A
NM_080686.2:c.5160+17G>A NP_542417.2:n.5160+17G>A
XM_011514890.1:c.5160+17G>A XP_011513192.1:n.5160+17G>A
XM_017011274.1:c.5160+17G>A XP_016866763.1:n.5160+17G>A
NM_004638.4:c.5160+17G>A MANE Select NP_004629.3:n.5160+17G>A
NM_080686.3:c.5160+17G>A NP_542417.2:n.5160+17G>A
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