Canonical Allele Identifier: CA10616764

Gene: PROS1

Linked Data

• ClinVar Variation Id: 346876
• ClinVar RCV Id: RCV000310852
• dbSNP Id: rs182088150
• gnomAD v2: 3-93592892-G-A
• gnomAD v3: 3-93874048-G-A
• gnomAD v4: 3-93874048-G-A
• MyVariant Identifiers: chr3:g.93592892G>A (hg19) ; chr3:g.93874048G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874048G>A , CM000665.2:g.93874048G>A	GRCh38
NC_000003.11:g.93592892G>A , CM000665.1:g.93592892G>A	GRCh37
NC_000003.10:g.95075582G>A	NCBI36
NG_009813.1:g.105043C>T , LRG_572:g.105043C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+196C>T	ENSP00000330021.7:n.*1+196C>T
ENST00000394236.9:c.*197C>T MANE Select	ENSP00000377783.3:n.*197C>T
ENST00000407433.6:c.*197C>T	ENSP00000385794.2:n.*197C>T
ENST00000647936.1:c.*331C>T	ENSP00000496822.1:n.*331C>T
ENST00000648381.1:n.2396C>T
ENST00000648853.1:c.*197C>T	ENSP00000497262.1:n.*197C>T
ENST00000650591.1:c.*197C>T	ENSP00000497376.1:n.*197C>T
ENST00000394236.7:c.*197C>T	ENSP00000377783.3:n.*197C>T
ENST00000407433.5:c.*197C>T	ENSP00000385794.1:n.*197C>T
NM_000313.3:c.*197C>T , LRG_572t1:c.*197C>T	NP_000304.2:n.*197C>T
NM_001314077.1:c.*197C>T , LRG_572t2:c.*197C>T	NP_001301006.1:n.*197C>T
NM_000313.4:c.*197C>T MANE Select	NP_000304.2:n.*197C>T
NM_001314077.2:c.*197C>T	NP_001301006.1:n.*197C>T