Canonical Allele Identifier: CA136852355
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1016675216
gnomAD v4: 6-31622664-T-C
MyVariant Identifiers: chr6:g.31590441T>C (hg19) chr6:g.31622664T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622664T>C , CM000668.2:g.31622664T>C GRCh38
NC_000006.11:g.31590441T>C , CM000668.1:g.31590441T>C GRCh37
NC_000006.10:g.31698420T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-100-26T>C MANE Select ENSP00000365201.2:n.-100-26T>C
ENST00000376007.8:c.-63-63T>C ENSP00000365175.4:n.-63-63T>C
ENST00000376033.2:c.-100-26T>C ENSP00000365201.2:n.-100-26T>C
ENST00000469577.5:n.136-1597T>C
NM_004638.3:c.-100-26T>C NP_004629.3:n.-100-26T>C
NM_080686.2:c.-63-63T>C NP_542417.2:n.-63-63T>C
XM_011514890.1:c.-63-63T>C XP_011513192.1:n.-63-63T>C
NM_004638.4:c.-100-26T>C MANE Select NP_004629.3:n.-100-26T>C
NM_080686.3:c.-63-63T>C NP_542417.2:n.-63-63T>C
Search 100 bp 5'
Search 100 bp 3'