Canonical Allele Identifier: CA2336421100
Gene: TGFB1 HGNC NCBI

Linked Data

dbSNP Id: rs201098266
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342152C>G , CM000681.2:g.41342152C>G GRCh38
NC_000019.9:g.41848057C>G , CM000681.1:g.41848057C>G GRCh37
NC_000019.8:g.46539897C>G NCBI36
NG_013364.1:g.16775G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000221930.6:c.712+18G>C MANE Select ENSP00000221930.4:n.712+18G>C
ENST00000600196.2:c.712+18G>C ENSP00000504008.1:n.712+18G>C
ENST00000677934.1:c.634+2595G>C ENSP00000504769.1:n.634+2595G>C
ENST00000221930.5:c.712+18G>C ENSP00000221930.4:n.712+18G>C
ENST00000597453.1:n.261G>C
ENST00000600196.1:n.172+18G>C
NM_000660.5:c.712+18G>C NP_000651.3:n.712+18G>C
XM_011527242.1:c.712+18G>C XP_011525544.1:n.712+18G>C
NM_000660.6:c.712+18G>C NP_000651.3:n.712+18G>C
XM_011527242.2:c.712+18G>C XP_011525544.1:n.712+18G>C
NM_000660.7:c.712+18G>C MANE Select NP_000651.3:n.712+18G>C
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