Canonical Allele Identifier: CA409755362
Gene: SOX18 HGNC NCBI
TCEA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.62680592A>T (hg19) chr20:g.64049239A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.64049239A>T , CM000682.2:g.64049239A>T GRCh38
NC_000020.10:g.62680592A>T , CM000682.1:g.62680592A>T GRCh37
NC_000020.9:g.62151036A>T NCBI36
NG_008095.1:g.5388T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340356.9:c.278T>A (SOX18) MANE Select ENSP00000341815.7:p.Met93Lys
ENST00000340356.8:c.278T>A (SOX18) ENSP00000341815.7:p.Met93Lys
NM_018419.2:c.278T>A (SOX18) NP_060889.1:p.Met93Lys
XM_011529022.1:c.-2320+6844A>T (TCEA2) XP_011527324.1:n.-2320+6844A>T
XM_011529025.1:c.-2236+6844A>T (TCEA2) XP_011527327.1:n.-2236+6844A>T
XM_024451978.1:c.-2236+6844A>T (TCEA2) XP_024307746.1:n.-2236+6844A>T
NM_018419.3:c.278T>A (SOX18) MANE Select NP_060889.1:p.Met93Lys
Search 100 bp 5'
Search 100 bp 3'