Canonical Allele Identifier: CA361039840

Gene: TGFBI

Linked Data

• gnomAD v4: 5-136055779-A-T
• MyVariant Identifiers: chr5:g.135391468A>T (hg19) ; chr5:g.136055779A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.136055779A>T , CM000667.2:g.136055779A>T	GRCh38
NC_000005.9:g.135391468A>T , CM000667.1:g.135391468A>T	GRCh37
NC_000005.8:g.135419367A>T	NCBI36
NG_012646.1:g.31885A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442011.7:c.1510A>T MANE Select	ENSP00000416330.2:p.Thr504Ser
ENST00000442011.6:c.1510A>T	ENSP00000416330.2:p.Thr504Ser
ENST00000506699.5:n.2027A>T
ENST00000507018.5:c.1488A>T
ENST00000509485.5:c.425A>T
ENST00000514242.5:n.281A>T
ENST00000514554.5:c.662A>T
NM_000358.2:c.1510A>T	NP_000349.1:p.Thr504Ser
NM_000358.3:c.1510A>T MANE Select	NP_000349.1:p.Thr504Ser