Canonical Allele Identifier: CA1926616778

Linked Data

dbSNP Id: rs1847040371

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.88989507T>C , CM000672.2:g.88989507T>C GRCh38
NC_000010.10:g.90749264T>C , CM000672.1:g.90749264T>C GRCh37
NC_000010.9:g.90739244T>C NCBI36
NG_009089.2:g.3977T>C , LRG_134:g.3977T>C
NG_011541.1:g.6884A>G , LRG_781:g.6884A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000415557.2:c.-24+1432A>G (ACTA2) ENSP00000396730.2:n.-24+1432A>G
ENST00000458159.6:c.-24+1515A>G (ACTA2) ENSP00000398239.2:n.-24+1515A>G
ENST00000696723.1:n.3591T>C (FAS)
ENST00000696992.1:n.1075T>C (FAS)
ENST00000688239.1:n.299T>C (FAS)
ENST00000690268.1:c.39T>C (FAS) ENSP00000509810.1:p.Gly13=
ENST00000415557.1:c.-24+1432A>G (ACTA2) ENSP00000396730.1:n.-24+1432A>G
ENST00000458159.5:c.-24+1515A>G (ACTA2) ENSP00000398239.1:n.-24+1515A>G
ENST00000458208.5:c.-24+1432A>G (ACTA2) ENSP00000402373.1:n.-24+1432A>G
NM_001141945.1:c.-24+1432A>G , LRG_781t2:c.-24+1432A>G (ACTA2) NP_001135417.1:n.-24+1432A>G
XM_006717819.2:c.39T>C (FAS) XP_006717882.1:p.Gly13=
XM_011539764.1:c.120T>C (FAS) XP_011538066.1:p.Gly40=
XM_011539765.1:c.120T>C (FAS) XP_011538067.1:p.Gly40=
XM_011539766.1:c.39T>C (FAS) XP_011538068.1:p.Gly13=
XM_011540016.1:c.-24+1515A>G (ACTA2) XP_011538318.1:n.-24+1515A>G
XR_945732.1:n.135T>C (FAS)
XR_945733.1:n.135T>C (FAS)
NM_001141945.2:c.-24+1432A>G (ACTA2) NP_001135417.1:n.-24+1432A>G
NM_001320855.1:c.-24+1515A>G (ACTA2) NP_001307784.1:n.-24+1515A>G
XM_006717819.3:c.39T>C (FAS) XP_006717882.1:p.Gly13=
XM_011539764.2:c.120T>C (FAS) XP_011538066.1:p.Gly40=
XM_011539765.2:c.120T>C (FAS) XP_011538067.1:p.Gly40=
XM_011539766.2:c.39T>C (FAS) XP_011538068.1:p.Gly13=
XR_945732.3:n.135T>C (FAS)
XR_945733.2:n.135T>C (FAS)