Canonical Allele Identifier: CA466158157
Gene: TMOD1 HGNC NCBI

Linked Data

dbSNP Id: rs1052270
MyVariant Identifiers: chr9:g.100275424C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97513142C>A , CM000671.2:g.97513142C>A GRCh38
NC_000009.11:g.100275424C>A , CM000671.1:g.100275424C>A GRCh37
NC_000009.10:g.99315245C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000259365.9:c.-48-10999C>A MANE Select ENSP00000259365.3:n.-48-10999C>A
ENST00000259365.8:c.-48-10999C>A ENSP00000259365.3:n.-48-10999C>A
ENST00000395211.6:c.-48-10999C>A ENSP00000378637.2:n.-48-10999C>A
NM_001166116.1:c.-48-10999C>A NP_001159588.1:n.-48-10999C>A
NM_003275.3:c.-48-10999C>A NP_003266.1:n.-48-10999C>A
XR_930157.1:n.902G>T
XM_024447660.1:c.-299-10999C>A XP_024303428.1:n.-299-10999C>A
XR_930157.2:n.827G>T
NM_003275.4:c.-48-10999C>A MANE Select NP_003266.1:n.-48-10999C>A
NM_001166116.2:c.-48-10999C>A NP_001159588.1:n.-48-10999C>A
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