Canonical Allele Identifier: CA343773614

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1166491615
• gnomAD v2: 1-173878759-T-G
• gnomAD v4: 1-173909621-T-G
• MyVariant Identifiers: chr1:g.173878759T>G (hg19) ; chr1:g.173909621T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909621T>G , CM000663.2:g.173909621T>G	GRCh38
NC_000001.10:g.173878759T>G , CM000663.1:g.173878759T>G	GRCh37
NC_000001.9:g.172145382T>G	NCBI36
NG_012462.1:g.12758A>C , LRG_577:g.12758A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1084A>C MANE Select	ENSP00000356671.3:p.Ser362Arg
ENST00000367698.3:c.1084A>C	ENSP00000356671.3:p.Ser362Arg
ENST00000617423.4:c.560-2128A>C	ENSP00000478688.1:n.560-2128A>C
NM_000488.3:c.1084A>C , LRG_577t1:c.1084A>C	NP_000479.1:p.Ser362Arg
XM_005245198.2:c.940A>C	XP_005245255.1:p.Ser314Arg
NM_001365052.1:c.940A>C	NP_001351981.1:p.Ser314Arg
NM_000488.4:c.1084A>C MANE Select	NP_000479.1:p.Ser362Arg
NM_001365052.2:c.940A>C	NP_001351981.1:p.Ser314Arg
NM_001386302.1:c.1207A>C	NP_001373231.1:p.Ser403Arg
NM_001386303.1:c.1165A>C	NP_001373232.1:p.Ser389Arg
NM_001386304.1:c.1063A>C	NP_001373233.1:p.Ser355Arg
NM_001386305.1:c.1027A>C	NP_001373234.1:p.Ser343Arg
NM_001386306.1:c.868A>C	NP_001373235.1:p.Ser290Arg