Canonical Allele Identifier: CA78484196
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs199469489
MyVariant Identifiers: chr3:g.93615617T>G (hg19) chr3:g.93896773T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93896773T>G , CM000665.2:g.93896773T>G GRCh38
NC_000003.11:g.93615617T>G , CM000665.1:g.93615617T>G GRCh37
NC_000003.10:g.95098307T>G NCBI36
NG_009813.1:g.82318A>C , LRG_572:g.82318A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.850-82A>C ENSP00000330021.7:n.850-82A>C
ENST00000394236.9:c.850-82A>C MANE Select ENSP00000377783.3:n.850-82A>C
ENST00000407433.6:c.805-82A>C ENSP00000385794.2:n.805-82A>C
ENST00000647936.1:c.850-82A>C ENSP00000496822.1:n.850-82A>C
ENST00000648381.1:n.1018-82A>C
ENST00000648853.1:c.808-82A>C ENSP00000497262.1:n.808-82A>C
ENST00000649103.1:c.949-82A>C ENSP00000497962.1:n.949-82A>C
ENST00000650591.1:c.946-82A>C ENSP00000497376.1:n.946-82A>C
ENST00000394236.7:c.850-82A>C ENSP00000377783.3:n.850-82A>C
ENST00000407433.5:c.457-82A>C ENSP00000385794.1:n.457-82A>C
NM_000313.3:c.850-82A>C , LRG_572t1:c.850-82A>C NP_000304.2:n.850-82A>C
NM_001314077.1:c.946-82A>C , LRG_572t2:c.946-82A>C NP_001301006.1:n.946-82A>C
NM_000313.4:c.850-82A>C MANE Select NP_000304.2:n.850-82A>C
NM_001314077.2:c.946-82A>C NP_001301006.1:n.946-82A>C
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