Canonical Allele Identifier: CA151970646
Gene: TTLL2 HGNC NCBI

Linked Data

dbSNP Id: rs879065850
MyVariant Identifiers: chr6:g.167755077T>A (hg19) chr6:g.167341589T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341589T>A , CM000668.2:g.167341589T>A GRCh38
NC_000006.11:g.167755077T>A , CM000668.1:g.167755077T>A GRCh37
NC_000006.10:g.167675067T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1689T>A MANE Select ENSP00000239587.5:p.Asn563Lys
ENST00000649884.1:c.1470T>A ENSP00000497040.1:p.Asn490Lys
ENST00000239587.9:c.1689T>A ENSP00000239587.5:p.Asn563Lys
ENST00000515138.1:c.1689T>A ENSP00000424130.1:p.Asn563Lys
NM_031949.4:c.1689T>A NP_114155.4:p.Asn563Lys
XM_006715572.2:c.1470T>A XP_006715635.1:p.Asn490Lys
XM_006715572.4:c.1470T>A XP_006715635.1:p.Asn490Lys
NM_031949.5:c.1689T>A MANE Select NP_114155.4:p.Asn563Lys
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