Canonical Allele Identifier: CA453305068
Gene: TTLL2 HGNC NCBI

Linked Data

dbSNP Id: rs1779085798
MyVariant Identifiers: chr6:g.167754609T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341121T>C , CM000668.2:g.167341121T>C GRCh38
NC_000006.11:g.167754609T>C , CM000668.1:g.167754609T>C GRCh37
NC_000006.10:g.167674599T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1221T>C MANE Select ENSP00000239587.5:p.Leu407=
ENST00000649884.1:c.1002T>C ENSP00000497040.1:p.Leu334=
ENST00000239587.9:c.1221T>C ENSP00000239587.5:p.Leu407=
ENST00000515138.1:c.1221T>C ENSP00000424130.1:p.Leu407=
NM_031949.4:c.1221T>C NP_114155.4:p.Leu407=
XM_006715572.2:c.1002T>C XP_006715635.1:p.Leu334=
XM_006715572.4:c.1002T>C XP_006715635.1:p.Leu334=
NM_031949.5:c.1221T>C MANE Select NP_114155.4:p.Leu407=
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