Canonical Allele Identifier: CA1221528068

Gene: TGFB2

Linked Data

• dbSNP Id: rs1571818991

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345698A>C , CM000663.2:g.218345698A>C	GRCh38
NC_000001.10:g.218519040A>C , CM000663.1:g.218519040A>C	GRCh37
NC_000001.9:g.216585663A>C	NCBI36
NG_027721.1:g.5365A>C
NG_027721.2:g.5365A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-1004A>C MANE Select	ENSP00000355897.4:n.-1004A>C
NM_001135599.2:c.-1004A>C	NP_001129071.1:n.-1004A>C
NM_003238.3:c.-1004A>C	NP_003229.1:n.-1004A>C
NM_001135599.3:c.-1004A>C	NP_001129071.1:n.-1004A>C
NM_003238.4:c.-1004A>C	NP_003229.1:n.-1004A>C
NR_138148.1:n.415A>C
NR_138149.1:n.415A>C
NM_003238.5:c.-1004A>C	NP_003229.1:n.-1004A>C
NM_003238.6:c.-1004A>C MANE Select	NP_003229.1:n.-1004A>C
NM_001135599.4:c.-1004A>C	NP_001129071.1:n.-1004A>C
NR_138148.2:n.363A>C
NR_138149.2:n.363A>C