Canonical Allele Identifier: CA3716860

Gene: PRRC2A

Linked Data

• dbSNP Id: rs769875014
• ExAC: 6:31605207 C / T
• gnomAD v2: 6-31605207-C-T
• gnomAD v4: 6-31637430-C-T
• MyVariant Identifiers: chr6:g.31605207C>T (hg19) ; chr6:g.31637430C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31637430C>T , CM000668.2:g.31637430C>T	GRCh38
NC_000006.11:g.31605207C>T , CM000668.1:g.31605207C>T	GRCh37
NC_000006.10:g.31713186C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.6334-16C>T MANE Select	ENSP00000365201.2:n.6334-16C>T
ENST00000376007.8:c.6334-16C>T	ENSP00000365175.4:n.6334-16C>T
ENST00000376033.2:c.6334-16C>T	ENSP00000365201.2:n.6334-16C>T
ENST00000462617.1:n.674C>T
ENST00000482441.1:n.394-16C>T
ENST00000492691.5:n.777C>T
NM_004638.3:c.6334-16C>T	NP_004629.3:n.6334-16C>T
NM_080686.2:c.6334-16C>T	NP_542417.2:n.6334-16C>T
XM_011514890.1:c.6121-16C>T	XP_011513192.1:n.6121-16C>T
XM_017011274.1:c.6121-16C>T	XP_016866763.1:n.6121-16C>T
NM_004638.4:c.6334-16C>T MANE Select	NP_004629.3:n.6334-16C>T
NM_080686.3:c.6334-16C>T	NP_542417.2:n.6334-16C>T