Canonical Allele Identifier: CA449662080
Gene: PRRC2A HGNC NCBI
SNORA38 HGNC NCBI

Linked Data

gnomAD v4: 6-31623108-C-A
MyVariant Identifiers: chr6:g.31590885C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31623108C>A , CM000668.2:g.31623108C>A GRCh38
NC_000006.11:g.31590885C>A , CM000668.1:g.31590885C>A GRCh37
NC_000006.10:g.31698864C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.112+207C>A (PRRC2A) MANE Select ENSP00000365201.2:n.112+207C>A
ENST00000376007.8:c.112+207C>A (PRRC2A) ENSP00000365175.4:n.112+207C>A
ENST00000376033.2:c.112+207C>A (PRRC2A) ENSP00000365201.2:n.112+207C>A
ENST00000469577.5:n.136-1153C>A (PRRC2A)
NM_004638.3:c.112+207C>A (PRRC2A) NP_004629.3:n.112+207C>A
NM_080686.2:c.112+207C>A (PRRC2A) NP_542417.2:n.112+207C>A
NR_002971.1:n.30C>A (SNORA38)
XM_011514890.1:c.112+207C>A (PRRC2A) XP_011513192.1:n.112+207C>A
XM_017011274.1:c.112+207C>A (PRRC2A) XP_016866763.1:n.112+207C>A
NM_004638.4:c.112+207C>A (PRRC2A) MANE Select NP_004629.3:n.112+207C>A
NM_080686.3:c.112+207C>A (PRRC2A) NP_542417.2:n.112+207C>A
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