Canonical Allele Identifier: CA32783319
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633231
ClinVar RCV Id: RCV003399991
dbSNP Id: rs199469508
MyVariant Identifiers: chr1:g.173886355A>G (hg19) chr1:g.173917217A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173917217A>G , CM000663.2:g.173917217A>G GRCh38
NC_000001.10:g.173886355A>G , CM000663.1:g.173886355A>G GRCh37
NC_000001.9:g.172152978A>G NCBI36
NG_012462.1:g.5162T>C , LRG_577:g.5162T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.41+2T>C MANE Select ENSP00000356671.3:n.41+2T>C
ENST00000367698.3:c.41+2T>C ENSP00000356671.3:n.41+2T>C
ENST00000494024.1:n.98+2T>C
ENST00000617423.4:c.41+2T>C ENSP00000478688.1:n.41+2T>C
NM_000488.3:c.41+2T>C , LRG_577t1:c.41+2T>C NP_000479.1:n.41+2T>C
XM_005245198.2:c.-273+2T>C XP_005245255.1:n.-273+2T>C
NM_001365052.1:c.-273+2T>C NP_001351981.1:n.-273+2T>C
NM_000488.4:c.41+2T>C MANE Select NP_000479.1:n.41+2T>C
NM_001365052.2:c.-273+2T>C NP_001351981.1:n.-273+2T>C
NM_001386302.1:c.41+2T>C NP_001373231.1:n.41+2T>C
NM_001386303.1:c.24+19T>C NP_001373232.1:n.24+19T>C
NM_001386304.1:c.41+2T>C NP_001373233.1:n.41+2T>C
NM_001386305.1:c.41+2T>C NP_001373234.1:n.41+2T>C
NM_001386306.1:c.41+2T>C NP_001373235.1:n.41+2T>C
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