Canonical Allele Identifier: CA823908636

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1231433516
• gnomAD v3: 6-31622695-A-C
• gnomAD v4: 6-31622695-A-C
• MyVariant Identifiers: chr6:g.31590472A>C (hg19) ; chr6:g.31622695A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622695A>C , CM000668.2:g.31622695A>C	GRCh38
NC_000006.11:g.31590472A>C , CM000668.1:g.31590472A>C	GRCh37
NC_000006.10:g.31698451A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.-95A>C MANE Select	ENSP00000365201.2:n.-95A>C
ENST00000376007.8:c.-63-32A>C	ENSP00000365175.4:n.-63-32A>C
ENST00000376033.2:c.-95A>C	ENSP00000365201.2:n.-95A>C
ENST00000469577.5:n.136-1566A>C
NM_004638.3:c.-95A>C	NP_004629.3:n.-95A>C
NM_080686.2:c.-63-32A>C	NP_542417.2:n.-63-32A>C
XM_011514890.1:c.-63-32A>C	XP_011513192.1:n.-63-32A>C
NM_004638.4:c.-95A>C MANE Select	NP_004629.3:n.-95A>C
NM_080686.3:c.-63-32A>C	NP_542417.2:n.-63-32A>C