Canonical Allele Identifier: CA136867697
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs947879333
gnomAD v2: 6-31602893-T-C
gnomAD v4: 6-31635116-T-C
MyVariant Identifiers: chr6:g.31602893T>C (hg19) chr6:g.31635116T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635116T>C , CM000668.2:g.31635116T>C GRCh38
NC_000006.11:g.31602893T>C , CM000668.1:g.31602893T>C GRCh37
NC_000006.10:g.31710872T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376033.3:c.5161-16T>C MANE Select ENSP00000365201.2:n.5161-16T>C
ENST00000376007.8:c.5161-16T>C ENSP00000365175.4:n.5161-16T>C
ENST00000376033.2:c.5161-16T>C ENSP00000365201.2:n.5161-16T>C
ENST00000484787.1:n.572-16T>C
NM_004638.3:c.5161-16T>C NP_004629.3:n.5161-16T>C
NM_080686.2:c.5161-16T>C NP_542417.2:n.5161-16T>C
XM_011514890.1:c.5161-16T>C XP_011513192.1:n.5161-16T>C
XM_017011274.1:c.5161-16T>C XP_016866763.1:n.5161-16T>C
NM_004638.4:c.5161-16T>C MANE Select NP_004629.3:n.5161-16T>C
NM_080686.3:c.5161-16T>C NP_542417.2:n.5161-16T>C
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