Canonical Allele Identifier: CA49795539

Gene: TGFA

Linked Data

• dbSNP Id: rs534566903
• gnomAD v4: 2-70450323-T-C
• MyVariant Identifiers: chr2:g.70677455T>C (hg19) ; chr2:g.70450323T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450323T>C , CM000664.2:g.70450323T>C	GRCh38
NC_000002.11:g.70677455T>C , CM000664.1:g.70677455T>C	GRCh37
NC_000002.10:g.70530963T>C	NCBI36
NG_029975.1:g.108693A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295400.11:c.*536A>G MANE Select	ENSP00000295400.6:n.*536A>G
ENST00000295400.10:c.*536A>G	ENSP00000295400.6:n.*536A>G
ENST00000418333.6:c.*536A>G	ENSP00000404099.2:n.*536A>G
ENST00000419940.5:c.379-702A>G
ENST00000445399.5:c.*19-702A>G	ENSP00000387493.1:n.*19-702A>G
NM_001099691.2:c.*536A>G	NP_001093161.1:n.*536A>G
NM_001308158.1:c.*536A>G	NP_001295087.1:n.*536A>G
NM_001308159.1:c.*536A>G	NP_001295088.1:n.*536A>G
NM_003236.3:c.*536A>G	NP_003227.1:n.*536A>G
NM_003236.4:c.*536A>G MANE Select	NP_003227.1:n.*536A>G
NM_001099691.3:c.*536A>G	NP_001093161.1:n.*536A>G
NM_001308158.2:c.*536A>G	NP_001295087.1:n.*536A>G
NM_001308159.2:c.*536A>G	NP_001295088.1:n.*536A>G