Canonical Allele Identifier: CA78520062

Gene: PROS1

Linked Data

• dbSNP Id: rs889132559
• gnomAD v2: 3-93592919-T-G
• gnomAD v3: 3-93874075-T-G
• gnomAD v4: 3-93874075-T-G
• MyVariant Identifiers: chr3:g.93592919T>G (hg19) ; chr3:g.93874075T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874075T>G , CM000665.2:g.93874075T>G	GRCh38
NC_000003.11:g.93592919T>G , CM000665.1:g.93592919T>G	GRCh37
NC_000003.10:g.95075609T>G	NCBI36
NG_009813.1:g.105016A>C , LRG_572:g.105016A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+169A>C	ENSP00000330021.7:n.*1+169A>C
ENST00000394236.9:c.*170A>C MANE Select	ENSP00000377783.3:n.*170A>C
ENST00000407433.6:c.*170A>C	ENSP00000385794.2:n.*170A>C
ENST00000647936.1:c.*304A>C	ENSP00000496822.1:n.*304A>C
ENST00000648381.1:n.2369A>C
ENST00000648853.1:c.*170A>C	ENSP00000497262.1:n.*170A>C
ENST00000650591.1:c.*170A>C	ENSP00000497376.1:n.*170A>C
ENST00000394236.7:c.*170A>C	ENSP00000377783.3:n.*170A>C
ENST00000407433.5:c.*170A>C	ENSP00000385794.1:n.*170A>C
NM_000313.3:c.*170A>C , LRG_572t1:c.*170A>C	NP_000304.2:n.*170A>C
NM_001314077.1:c.*170A>C , LRG_572t2:c.*170A>C	NP_001301006.1:n.*170A>C
NM_000313.4:c.*170A>C MANE Select	NP_000304.2:n.*170A>C
NM_001314077.2:c.*170A>C	NP_001301006.1:n.*170A>C