Canonical Allele Identifier: CA353670484
Gene: PROS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 429810
ClinVar RCV Id: RCV000493409
dbSNP Id: rs1131691605
MyVariant Identifiers: chr3:g.93605348C>T (hg19) chr3:g.93886504C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93886504C>T , CM000665.2:g.93886504C>T GRCh38
NC_000003.11:g.93605348C>T , CM000665.1:g.93605348C>T GRCh37
NC_000003.10:g.95088038C>T NCBI36
NG_009813.1:g.92587G>A , LRG_572:g.92587G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.1156-1G>A ENSP00000330021.7:n.1156-1G>A
ENST00000394236.9:c.1156-1G>A MANE Select ENSP00000377783.3:n.1156-1G>A
ENST00000407433.6:c.1111-1G>A ENSP00000385794.2:n.1111-1G>A
ENST00000647936.1:c.1156-1G>A ENSP00000496822.1:n.1156-1G>A
ENST00000648381.1:n.1324-1G>A
ENST00000648853.1:c.1114-1G>A ENSP00000497262.1:n.1114-1G>A
ENST00000649103.1:c.1255-1G>A ENSP00000497962.1:n.1255-1G>A
ENST00000650591.1:c.1252-1G>A ENSP00000497376.1:n.1252-1G>A
ENST00000394236.7:c.1156-1G>A ENSP00000377783.3:n.1156-1G>A
ENST00000407433.5:c.763-1G>A ENSP00000385794.1:n.763-1G>A
NM_000313.3:c.1156-1G>A , LRG_572t1:c.1156-1G>A NP_000304.2:n.1156-1G>A
NM_001314077.1:c.1252-1G>A , LRG_572t2:c.1252-1G>A NP_001301006.1:n.1252-1G>A
NM_000313.4:c.1156-1G>A MANE Select NP_000304.2:n.1156-1G>A
NM_001314077.2:c.1252-1G>A NP_001301006.1:n.1252-1G>A
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