Canonical Allele Identifier: CA9460015

Gene: TGFB1

Linked Data

• dbSNP Id: rs760353294
• ExAC: 19:41848026 C / T
• gnomAD v2: 19-41848026-C-T
• gnomAD v4: 19-41342121-C-T
• MyVariant Identifiers: chr19:g.41848026C>T (hg19) ; chr19:g.41342121C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342121C>T , CM000681.2:g.41342121C>T	GRCh38
NC_000019.9:g.41848026C>T , CM000681.1:g.41848026C>T	GRCh37
NC_000019.8:g.46539866C>T	NCBI36
NG_013364.1:g.16806G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.712+49G>A MANE Select	ENSP00000221930.4:n.712+49G>A
ENST00000600196.2:c.712+49G>A	ENSP00000504008.1:n.712+49G>A
ENST00000677934.1:c.634+2626G>A	ENSP00000504769.1:n.634+2626G>A
ENST00000221930.5:c.712+49G>A	ENSP00000221930.4:n.712+49G>A
ENST00000597453.1:n.292G>A
ENST00000600196.1:n.172+49G>A
NM_000660.5:c.712+49G>A	NP_000651.3:n.712+49G>A
XM_011527242.1:c.712+49G>A	XP_011525544.1:n.712+49G>A
NM_000660.6:c.712+49G>A	NP_000651.3:n.712+49G>A
XM_011527242.2:c.712+49G>A	XP_011525544.1:n.712+49G>A
NM_000660.7:c.712+49G>A MANE Select	NP_000651.3:n.712+49G>A