Canonical Allele Identifier: CA2677997146
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31623040-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31623040C>G , CM000668.2:g.31623040C>G GRCh38
NC_000006.11:g.31590817C>G , CM000668.1:g.31590817C>G GRCh37
NC_000006.10:g.31698796C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376033.3:c.112+139C>G MANE Select ENSP00000365201.2:n.112+139C>G
ENST00000376007.8:c.112+139C>G ENSP00000365175.4:n.112+139C>G
ENST00000376033.2:c.112+139C>G ENSP00000365201.2:n.112+139C>G
ENST00000469577.5:n.136-1221C>G
NM_004638.3:c.112+139C>G NP_004629.3:n.112+139C>G
NM_080686.2:c.112+139C>G NP_542417.2:n.112+139C>G
XM_011514890.1:c.112+139C>G XP_011513192.1:n.112+139C>G
XM_017011274.1:c.112+139C>G XP_016866763.1:n.112+139C>G
NM_004638.4:c.112+139C>G MANE Select NP_004629.3:n.112+139C>G
NM_080686.3:c.112+139C>G NP_542417.2:n.112+139C>G
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