Canonical Allele Identifier: CA344725586

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218346937-A-C
• MyVariant Identifiers: chr1:g.218520279A>C (hg19) ; chr1:g.218346937A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346937A>C , CM000663.2:g.218346937A>C	GRCh38
NC_000001.10:g.218520279A>C , CM000663.1:g.218520279A>C	GRCh37
NC_000001.9:g.216586902A>C	NCBI36
NG_027721.1:g.6604A>C
NG_027721.2:g.6604A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.236A>C MANE Select	ENSP00000355897.4:p.Gln79Pro
ENST00000366929.4:c.236A>C	ENSP00000355896.4:p.Gln79Pro
ENST00000366930.8:c.236A>C	ENSP00000355897.4:p.Gln79Pro
NM_001135599.2:c.236A>C	NP_001129071.1:p.Gln79Pro
NM_003238.3:c.236A>C	NP_003229.1:p.Gln79Pro
NM_001135599.3:c.236A>C	NP_001129071.1:p.Gln79Pro
NM_003238.4:c.236A>C	NP_003229.1:p.Gln79Pro
NR_138148.1:n.1654A>C
NR_138149.1:n.1654A>C
NM_003238.5:c.236A>C	NP_003229.1:p.Gln79Pro
NM_003238.6:c.236A>C MANE Select	NP_003229.1:p.Gln79Pro
NM_001135599.4:c.236A>C	NP_001129071.1:p.Gln79Pro
NR_138148.2:n.1602A>C
NR_138149.2:n.1602A>C