Canonical Allele Identifier: CA527299897

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1247723854
• gnomAD v2: 1-173880430-G-C
• gnomAD v3: 1-173911292-G-C
• gnomAD v4: 1-173911292-G-C
• MyVariant Identifiers: chr1:g.173880430G>C (hg19) ; chr1:g.173911292G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911292G>C , CM000663.2:g.173911292G>C	GRCh38
NC_000001.10:g.173880430G>C , CM000663.1:g.173880430G>C	GRCh37
NC_000001.9:g.172147053G>C	NCBI36
NG_012462.1:g.11087C>G , LRG_577:g.11087C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.625-401C>G MANE Select	ENSP00000356671.3:n.625-401C>G
ENST00000367698.3:c.625-401C>G	ENSP00000356671.3:n.625-401C>G
ENST00000487183.1:n.330-455C>G
ENST00000617423.4:c.559+572C>G	ENSP00000478688.1:n.559+572C>G
NM_000488.3:c.625-401C>G , LRG_577t1:c.625-401C>G	NP_000479.1:n.625-401C>G
XM_005245198.2:c.481-401C>G	XP_005245255.1:n.481-401C>G
NM_001365052.1:c.481-401C>G	NP_001351981.1:n.481-401C>G
NM_000488.4:c.625-401C>G MANE Select	NP_000479.1:n.625-401C>G
NM_001365052.2:c.481-401C>G	NP_001351981.1:n.481-401C>G
NM_001386302.1:c.625-401C>G	NP_001373231.1:n.625-401C>G
NM_001386303.1:c.706-401C>G	NP_001373232.1:n.706-401C>G
NM_001386304.1:c.625-401C>G	NP_001373233.1:n.625-401C>G
NM_001386305.1:c.625-401C>G	NP_001373234.1:n.625-401C>G
NM_001386306.1:c.409-401C>G	NP_001373235.1:n.409-401C>G