Canonical Allele Identifier: CA823908627
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1211436180
gnomAD v3: 6-31622681-T-C
gnomAD v4: 6-31622681-T-C
MyVariant Identifiers: chr6:g.31590458T>C (hg19) chr6:g.31622681T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622681T>C , CM000668.2:g.31622681T>C GRCh38
NC_000006.11:g.31590458T>C , CM000668.1:g.31590458T>C GRCh37
NC_000006.10:g.31698437T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-100-9T>C MANE Select ENSP00000365201.2:n.-100-9T>C
ENST00000376007.8:c.-63-46T>C ENSP00000365175.4:n.-63-46T>C
ENST00000376033.2:c.-100-9T>C ENSP00000365201.2:n.-100-9T>C
ENST00000469577.5:n.136-1580T>C
NM_004638.3:c.-100-9T>C NP_004629.3:n.-100-9T>C
NM_080686.2:c.-63-46T>C NP_542417.2:n.-63-46T>C
XM_011514890.1:c.-63-46T>C XP_011513192.1:n.-63-46T>C
NM_004638.4:c.-100-9T>C MANE Select NP_004629.3:n.-100-9T>C
NM_080686.3:c.-63-46T>C NP_542417.2:n.-63-46T>C
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