Canonical Allele Identifier: CA1385026849
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs1576170396
gnomAD v4: 3-93874172-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874172C>T , CM000665.2:g.93874172C>T GRCh38
NC_000003.11:g.93593016C>T , CM000665.1:g.93593016C>T GRCh37
NC_000003.10:g.95075706C>T NCBI36
NG_009813.1:g.104919G>A , LRG_572:g.104919G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.*1+72G>A ENSP00000330021.7:n.*1+72G>A
ENST00000394236.9:c.*73G>A MANE Select ENSP00000377783.3:n.*73G>A
ENST00000407433.6:c.*73G>A ENSP00000385794.2:n.*73G>A
ENST00000647936.1:c.*207G>A ENSP00000496822.1:n.*207G>A
ENST00000648381.1:n.2272G>A
ENST00000648853.1:c.*73G>A ENSP00000497262.1:n.*73G>A
ENST00000650591.1:c.*73G>A ENSP00000497376.1:n.*73G>A
ENST00000394236.7:c.*73G>A ENSP00000377783.3:n.*73G>A
ENST00000407433.5:c.*73G>A ENSP00000385794.1:n.*73G>A
NM_000313.3:c.*73G>A , LRG_572t1:c.*73G>A NP_000304.2:n.*73G>A
NM_001314077.1:c.*73G>A , LRG_572t2:c.*73G>A NP_001301006.1:n.*73G>A
NM_000313.4:c.*73G>A MANE Select NP_000304.2:n.*73G>A
NM_001314077.2:c.*73G>A NP_001301006.1:n.*73G>A
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