Canonical Allele Identifier: CA453090879
Gene: TTLL2 HGNC NCBI

Linked Data

dbSNP Id: rs2115228347
COSMIC: COSM1311812
MyVariant Identifiers: chr6:g.167755014G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341526G>C , CM000668.2:g.167341526G>C GRCh38
NC_000006.11:g.167755014G>C , CM000668.1:g.167755014G>C GRCh37
NC_000006.10:g.167675004G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1626G>C MANE Select ENSP00000239587.5:p.Leu542=
ENST00000649884.1:c.1407G>C ENSP00000497040.1:p.Leu469=
ENST00000239587.9:c.1626G>C ENSP00000239587.5:p.Leu542=
ENST00000515138.1:c.1626G>C ENSP00000424130.1:p.Leu542=
NM_031949.4:c.1626G>C NP_114155.4:p.Leu542=
XM_006715572.2:c.1407G>C XP_006715635.1:p.Leu469=
XM_006715572.4:c.1407G>C XP_006715635.1:p.Leu469=
NM_031949.5:c.1626G>C MANE Select NP_114155.4:p.Leu542=
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