Canonical Allele Identifier: CA366425086
Gene: TTLL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.167755072T>G (hg19) chr6:g.167341584T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341584T>G , CM000668.2:g.167341584T>G GRCh38
NC_000006.11:g.167755072T>G , CM000668.1:g.167755072T>G GRCh37
NC_000006.10:g.167675062T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1684T>G MANE Select ENSP00000239587.5:p.Phe562Val
ENST00000649884.1:c.1465T>G ENSP00000497040.1:p.Phe489Val
ENST00000239587.9:c.1684T>G ENSP00000239587.5:p.Phe562Val
ENST00000515138.1:c.1684T>G ENSP00000424130.1:p.Phe562Val
NM_031949.4:c.1684T>G NP_114155.4:p.Phe562Val
XM_006715572.2:c.1465T>G XP_006715635.1:p.Phe489Val
XM_006715572.4:c.1465T>G XP_006715635.1:p.Phe489Val
NM_031949.5:c.1684T>G MANE Select NP_114155.4:p.Phe562Val
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