Canonical Allele Identifier: CA223254013
Gene: TCN1 HGNC NCBI

Linked Data

dbSNP Id: rs528852650
gnomAD v3: 11-59865944-C-A
gnomAD v4: 11-59865944-C-A
MyVariant Identifiers: chr11:g.59633417C>A (hg19) chr11:g.59865944C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.59865944C>A , CM000673.2:g.59865944C>A GRCh38
NC_000011.9:g.59633417C>A , CM000673.1:g.59633417C>A GRCh37
NC_000011.8:g.59389993C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000257264.4:c.79+448G>T MANE Select ENSP00000257264.3:n.79+448G>T
ENST00000257264.3:c.79+448G>T ENSP00000257264.3:n.79+448G>T
ENST00000532419.5:n.98+448G>T
ENST00000534531.1:n.80+448G>T
NM_001062.3:c.79+448G>T NP_001053.2:n.79+448G>T
NM_001062.4:c.79+448G>T MANE Select NP_001053.2:n.79+448G>T
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