Canonical Allele Identifier: CA2650531269

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218346669-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346669T>C , CM000663.2:g.218346669T>C	GRCh38
NC_000001.10:g.218520011T>C , CM000663.1:g.218520011T>C	GRCh37
NC_000001.9:g.216586634T>C	NCBI36
NG_027721.1:g.6336T>C
NG_027721.2:g.6336T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-33T>C MANE Select	ENSP00000355897.4:n.-33T>C
ENST00000366929.4:c.-33T>C	ENSP00000355896.4:n.-33T>C
ENST00000366930.8:c.-33T>C	ENSP00000355897.4:n.-33T>C
NM_001135599.2:c.-33T>C	NP_001129071.1:n.-33T>C
NM_003238.3:c.-33T>C	NP_003229.1:n.-33T>C
NM_001135599.3:c.-33T>C	NP_001129071.1:n.-33T>C
NM_003238.4:c.-33T>C	NP_003229.1:n.-33T>C
NR_138148.1:n.1386T>C
NR_138149.1:n.1386T>C
NM_003238.5:c.-33T>C	NP_003229.1:n.-33T>C
NM_003238.6:c.-33T>C MANE Select	NP_003229.1:n.-33T>C
NM_001135599.4:c.-33T>C	NP_001129071.1:n.-33T>C
NR_138148.2:n.1334T>C
NR_138149.2:n.1334T>C