Canonical Allele Identifier: CA409755400
Gene: SOX18 HGNC NCBI
TCEA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.62680600G>C (hg19) chr20:g.64049247G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.64049247G>C , CM000682.2:g.64049247G>C GRCh38
NC_000020.10:g.62680600G>C , CM000682.1:g.62680600G>C GRCh37
NC_000020.9:g.62151044G>C NCBI36
NG_008095.1:g.5380C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000340356.9:c.270C>G (SOX18) MANE Select ENSP00000341815.7:p.Asn90Lys
ENST00000340356.8:c.270C>G (SOX18) ENSP00000341815.7:p.Asn90Lys
NM_018419.2:c.270C>G (SOX18) NP_060889.1:p.Asn90Lys
XM_011529022.1:c.-2320+6852G>C (TCEA2) XP_011527324.1:n.-2320+6852G>C
XM_011529025.1:c.-2236+6852G>C (TCEA2) XP_011527327.1:n.-2236+6852G>C
XM_024451978.1:c.-2236+6852G>C (TCEA2) XP_024307746.1:n.-2236+6852G>C
NM_018419.3:c.270C>G (SOX18) MANE Select NP_060889.1:p.Asn90Lys
Search 100 bp 5'
Search 100 bp 3'