Canonical Allele Identifier: CA11188976
Gene: TGFA HGNC NCBI
TGFA-IT1 HGNC NCBI

Linked Data

dbSNP Id: rs3771514
gnomAD v2: 2-70697667-G-A
gnomAD v3: 2-70470535-G-A
gnomAD v4: 2-70470535-G-A
MyVariant Identifiers: chr2:g.70697667G>A (hg19) chr2:g.70470535G>A (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70470535G>A , CM000664.2:g.70470535G>A GRCh38
NC_000002.11:g.70697667G>A , CM000664.1:g.70697667G>A GRCh37
NC_000002.10:g.70551175G>A NCBI36
NG_029975.1:g.88481C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295400.11:c.95-4799C>T (TGFA) MANE Select ENSP00000295400.6:n.95-4799C>T
ENST00000295400.10:c.95-4799C>T (TGFA) ENSP00000295400.6:n.95-4799C>T
ENST00000394241.3:c.95-4802C>T (TGFA) ENSP00000377787.3:n.95-4802C>T
ENST00000418333.6:c.95-4802C>T (TGFA) ENSP00000404099.2:n.95-4802C>T
ENST00000444975.5:c.113-4799C>T (TGFA) ENSP00000404131.1:n.113-4799C>T
ENST00000445399.5:c.95-4802C>T (TGFA) ENSP00000387493.1:n.95-4802C>T
ENST00000450929.5:c.113-4802C>T (TGFA) ENSP00000414127.1:n.113-4802C>T
ENST00000460808.5:n.154-4799C>T (TGFA)
NM_001099691.2:c.95-4802C>T (TGFA) NP_001093161.1:n.95-4802C>T
NM_001308158.1:c.113-4799C>T (TGFA) NP_001295087.1:n.113-4799C>T
NM_001308159.1:c.113-4802C>T (TGFA) NP_001295088.1:n.113-4802C>T
NM_003236.3:c.95-4799C>T (TGFA) NP_003227.1:n.95-4799C>T
NR_046798.1:n.57-2040C>T (TGFA-IT1)
NM_003236.4:c.95-4799C>T (TGFA) MANE Select NP_003227.1:n.95-4799C>T
NM_001099691.3:c.95-4802C>T (TGFA) NP_001093161.1:n.95-4802C>T
NM_001308158.2:c.113-4799C>T (TGFA) NP_001295087.1:n.113-4799C>T
NM_001308159.2:c.113-4802C>T (TGFA) NP_001295088.1:n.113-4802C>T
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