Canonical Allele Identifier: CA421942878

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1657677278
• MyVariant Identifiers: chr1:g.173878790G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909652G>A , CM000663.2:g.173909652G>A	GRCh38
NC_000001.10:g.173878790G>A , CM000663.1:g.173878790G>A	GRCh37
NC_000001.9:g.172145413G>A	NCBI36
NG_012462.1:g.12727C>T , LRG_577:g.12727C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1053C>T MANE Select	ENSP00000356671.3:p.His351=
ENST00000367698.3:c.1053C>T	ENSP00000356671.3:p.His351=
ENST00000617423.4:c.560-2159C>T	ENSP00000478688.1:n.560-2159C>T
NM_000488.3:c.1053C>T , LRG_577t1:c.1053C>T	NP_000479.1:p.His351=
XM_005245198.2:c.909C>T	XP_005245255.1:p.His303=
NM_001365052.1:c.909C>T	NP_001351981.1:p.His303=
NM_000488.4:c.1053C>T MANE Select	NP_000479.1:p.His351=
NM_001365052.2:c.909C>T	NP_001351981.1:p.His303=
NM_001386302.1:c.1176C>T	NP_001373231.1:p.His392=
NM_001386303.1:c.1134C>T	NP_001373232.1:p.His378=
NM_001386304.1:c.1032C>T	NP_001373233.1:p.His344=
NM_001386305.1:c.996C>T	NP_001373234.1:p.His332=
NM_001386306.1:c.837C>T	NP_001373235.1:p.His279=