Canonical Allele Identifier: CA1009276532

Gene: SERPINC1

Linked Data

• dbSNP Id: rs2102780464
• gnomAD v3: 1-173908405-A-G
• gnomAD v4: 1-173908405-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173908405A>G , CM000663.2:g.173908405A>G	GRCh38
NC_000001.10:g.173877543A>G , CM000663.1:g.173877543A>G	GRCh37
NC_000001.9:g.172144166A>G	NCBI36
NG_012462.1:g.13974T>C , LRG_577:g.13974T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1154-891T>C MANE Select	ENSP00000356671.3:n.1154-891T>C
ENST00000367698.3:c.1154-891T>C	ENSP00000356671.3:n.1154-891T>C
ENST00000617423.4:c.560-912T>C	ENSP00000478688.1:n.560-912T>C
NM_000488.3:c.1154-891T>C , LRG_577t1:c.1154-891T>C	NP_000479.1:n.1154-891T>C
XM_005245198.2:c.1010-891T>C	XP_005245255.1:n.1010-891T>C
NM_001365052.1:c.1010-891T>C	NP_001351981.1:n.1010-891T>C
NM_000488.4:c.1154-891T>C MANE Select	NP_000479.1:n.1154-891T>C
NM_001365052.2:c.1010-891T>C	NP_001351981.1:n.1010-891T>C
NM_001386302.1:c.1277-891T>C	NP_001373231.1:n.1277-891T>C
NM_001386303.1:c.1235-891T>C	NP_001373232.1:n.1235-891T>C
NM_001386304.1:c.1133-891T>C	NP_001373233.1:n.1133-891T>C
NM_001386305.1:c.1097-891T>C	NP_001373234.1:n.1097-891T>C
NM_001386306.1:c.938-891T>C	NP_001373235.1:n.938-891T>C