Canonical Allele Identifier: CA566355374
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1222913444
gnomAD v2: 6-31590491-G-C
gnomAD v3: 6-31622714-G-C
gnomAD v4: 6-31622714-G-C
MyVariant Identifiers: chr6:g.31590491G>C (hg19) chr6:g.31622714G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622714G>C , CM000668.2:g.31622714G>C GRCh38
NC_000006.11:g.31590491G>C , CM000668.1:g.31590491G>C GRCh37
NC_000006.10:g.31698470G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-76G>C MANE Select ENSP00000365201.2:n.-76G>C
ENST00000376007.8:c.-63-13G>C ENSP00000365175.4:n.-63-13G>C
ENST00000376033.2:c.-76G>C ENSP00000365201.2:n.-76G>C
ENST00000469577.5:n.136-1547G>C
NM_004638.3:c.-76G>C NP_004629.3:n.-76G>C
NM_080686.2:c.-63-13G>C NP_542417.2:n.-63-13G>C
XM_011514890.1:c.-63-13G>C XP_011513192.1:n.-63-13G>C
NM_004638.4:c.-76G>C MANE Select NP_004629.3:n.-76G>C
NM_080686.3:c.-63-13G>C NP_542417.2:n.-63-13G>C
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