Canonical Allele Identifier: CA11307593
Gene: SERPINE2 HGNC NCBI

Linked Data

dbSNP Id: rs6734100
gnomAD v2: 2-224841995-C-G
gnomAD v3: 2-223977278-C-G
gnomAD v4: 2-223977278-C-G
MyVariant Identifiers: chr2:g.224841995C>G (hg19) chr2:g.223977278C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223977278C>G , CM000664.2:g.223977278C>G GRCh38
NC_000002.11:g.224841995C>G , CM000664.1:g.224841995C>G GRCh37
NC_000002.10:g.224550239C>G NCBI36
NG_032907.1:g.67042G>C
NG_032907.2:g.67042G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258405.9:c.1159+266G>C ENSP00000258405.4:n.1159+266G>C
ENST00000409304.6:c.1156+266G>C MANE Select ENSP00000386412.1:n.1156+266G>C
ENST00000258405.8:c.1159+266G>C ENSP00000258405.4:n.1159+266G>C
ENST00000409304.5:c.1156+266G>C ENSP00000386412.1:n.1156+266G>C
ENST00000409840.7:c.1156+266G>C ENSP00000386969.3:n.1156+266G>C
ENST00000447280.6:c.1192+266G>C ENSP00000415786.2:n.1192+266G>C
ENST00000473202.1:n.5237+266G>C
ENST00000478966.1:n.589+266G>C
NM_001136528.1:c.1156+266G>C NP_001130000.1:n.1156+266G>C
NM_001136530.1:c.1192+266G>C NP_001130002.1:n.1192+266G>C
NM_006216.3:c.1159+266G>C NP_006207.1:n.1159+266G>C
NR_073116.1:n.1817+266G>C
XM_005246641.2:c.1195+266G>C XP_005246698.1:n.1195+266G>C
XM_005246642.2:c.1159+266G>C XP_005246699.1:n.1159+266G>C
XM_017004330.1:c.1159+266G>C XP_016859819.1:n.1159+266G>C
XM_017004332.2:c.1156+266G>C XP_016859821.1:n.1156+266G>C
NM_001136528.2:c.1156+266G>C MANE Select NP_001130000.1:n.1156+266G>C
NM_006216.4:c.1159+266G>C NP_006207.1:n.1159+266G>C
NR_073116.2:n.1817+266G>C
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