Canonical Allele Identifier: CA1619235474
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs972630980
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622931G>C , CM000668.2:g.31622931G>C GRCh38
NC_000006.11:g.31590708G>C , CM000668.1:g.31590708G>C GRCh37
NC_000006.10:g.31698687G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.112+30G>C MANE Select ENSP00000365201.2:n.112+30G>C
ENST00000376007.8:c.112+30G>C ENSP00000365175.4:n.112+30G>C
ENST00000376033.2:c.112+30G>C ENSP00000365201.2:n.112+30G>C
ENST00000469577.5:n.136-1330G>C
NM_004638.3:c.112+30G>C NP_004629.3:n.112+30G>C
NM_080686.2:c.112+30G>C NP_542417.2:n.112+30G>C
XM_011514890.1:c.112+30G>C XP_011513192.1:n.112+30G>C
XM_017011274.1:c.112+30G>C XP_016866763.1:n.112+30G>C
NM_004638.4:c.112+30G>C MANE Select NP_004629.3:n.112+30G>C
NM_080686.3:c.112+30G>C NP_542417.2:n.112+30G>C
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