Canonical Allele Identifier: CA7280290

Linked Data

dbSNP Id: rs775311850

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75961034G>A , CM000676.2:g.75961034G>A GRCh38
NC_000014.8:g.76427377G>A , CM000676.1:g.76427377G>A GRCh37
NC_000014.7:g.75497130G>A NCBI36
NG_011715.1:g.25716C>T , LRG_399:g.25716C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000238682.8:c.969C>T (TGFB3) MANE Select ENSP00000238682.3:p.Asp323=
ENST00000556674.2:c.969C>T (TGFB3) ENSP00000502685.1:p.Asp323=
ENST00000238682.7:c.969C>T (TGFB3) ENSP00000238682.3:p.Asp323=
ENST00000554980.5:n.1350C>T (TGFB3)
ENST00000555677.5:n.90-27851G>A (IFT43)
ENST00000557493.1:n.435C>T (TGFB3)
NM_003239.3:c.969C>T (TGFB3) NP_003230.1:p.Asp323=
XM_005268028.1:c.969C>T (TGFB3) XP_005268085.1:p.Asp323=
NM_001329939.1:c.969C>T (TGFB3) NP_001316868.1:p.Asp323=
NM_003239.4:c.969C>T (TGFB3) NP_003230.1:p.Asp323=
NM_001329939.2:c.969C>T (TGFB3) NP_001316868.1:p.Asp323=
NM_003239.5:c.969C>T (TGFB3) MANE Select NP_003230.1:p.Asp323=