Canonical Allele Identifier: CA363332195
Gene: PRRC2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31590675G>C (hg19) chr6:g.31622898G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622898G>C , CM000668.2:g.31622898G>C GRCh38
NC_000006.11:g.31590675G>C , CM000668.1:g.31590675G>C GRCh37
NC_000006.10:g.31698654G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.109G>C MANE Select ENSP00000365201.2:p.Ala37Pro
ENST00000376007.8:c.109G>C ENSP00000365175.4:p.Ala37Pro
ENST00000376033.2:c.109G>C ENSP00000365201.2:p.Ala37Pro
ENST00000469577.5:n.136-1363G>C
NM_004638.3:c.109G>C NP_004629.3:p.Ala37Pro
NM_080686.2:c.109G>C NP_542417.2:p.Ala37Pro
XM_011514890.1:c.109G>C XP_011513192.1:p.Ala37Pro
XM_017011274.1:c.109G>C XP_016866763.1:p.Ala37Pro
NM_004638.4:c.109G>C MANE Select NP_004629.3:p.Ala37Pro
NM_080686.3:c.109G>C NP_542417.2:p.Ala37Pro
Search 100 bp 5'
Search 100 bp 3'