Canonical Allele Identifier: CA136852413

Gene: PRRC2A

Linked Data

• dbSNP Id: rs543397473
• gnomAD v3: 6-31622717-T-C
• gnomAD v4: 6-31622717-T-C
• MyVariant Identifiers: chr6:g.31590494T>C (hg19) ; chr6:g.31622717T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622717T>C , CM000668.2:g.31622717T>C	GRCh38
NC_000006.11:g.31590494T>C , CM000668.1:g.31590494T>C	GRCh37
NC_000006.10:g.31698473T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.-73T>C MANE Select	ENSP00000365201.2:n.-73T>C
ENST00000376007.8:c.-63-10T>C	ENSP00000365175.4:n.-63-10T>C
ENST00000376033.2:c.-73T>C	ENSP00000365201.2:n.-73T>C
ENST00000469577.5:n.136-1544T>C
NM_004638.3:c.-73T>C	NP_004629.3:n.-73T>C
NM_080686.2:c.-63-10T>C	NP_542417.2:n.-63-10T>C
XM_011514890.1:c.-63-10T>C	XP_011513192.1:n.-63-10T>C
NM_004638.4:c.-73T>C MANE Select	NP_004629.3:n.-73T>C
NM_080686.3:c.-63-10T>C	NP_542417.2:n.-63-10T>C