Canonical Allele Identifier: CA1619235168
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs972387526
gnomAD v4: 6-31622713-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622713T>G , CM000668.2:g.31622713T>G GRCh38
NC_000006.11:g.31590490T>G , CM000668.1:g.31590490T>G GRCh37
NC_000006.10:g.31698469T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-77T>G MANE Select ENSP00000365201.2:n.-77T>G
ENST00000376007.8:c.-63-14T>G ENSP00000365175.4:n.-63-14T>G
ENST00000376033.2:c.-77T>G ENSP00000365201.2:n.-77T>G
ENST00000469577.5:n.136-1548T>G
NM_004638.3:c.-77T>G NP_004629.3:n.-77T>G
NM_080686.2:c.-63-14T>G NP_542417.2:n.-63-14T>G
XM_011514890.1:c.-63-14T>G XP_011513192.1:n.-63-14T>G
NM_004638.4:c.-77T>G MANE Select NP_004629.3:n.-77T>G
NM_080686.3:c.-63-14T>G NP_542417.2:n.-63-14T>G
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