Canonical Allele Identifier: CA30788016
Gene: TPM3 HGNC NCBI

Linked Data

dbSNP Id: rs555013085
gnomAD v2: 1-154164617-T-C
gnomAD v3: 1-154192141-T-C
gnomAD v4: 1-154192141-T-C
MyVariant Identifiers: chr1:g.154164617T>C (hg19) chr1:g.154192141T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154192141T>C , CM000663.2:g.154192141T>C GRCh38
NC_000001.10:g.154164617T>C , CM000663.1:g.154164617T>C GRCh37
NC_000001.9:g.152431241T>C NCBI36
NG_008621.1:g.4993A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368530.6:c.-123A>G ENSP00000357516.2:n.-123A>G
ENST00000515609.1:c.-49-74A>G ENSP00000426306.1:n.-49-74A>G
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