Canonical Allele Identifier: CA151970626
Gene: TTLL2 HGNC NCBI

Linked Data

dbSNP Id: rs866719140
MyVariant Identifiers: chr6:g.167755055T>A (hg19) chr6:g.167341567T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341567T>A , CM000668.2:g.167341567T>A GRCh38
NC_000006.11:g.167755055T>A , CM000668.1:g.167755055T>A GRCh37
NC_000006.10:g.167675045T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1667T>A MANE Select ENSP00000239587.5:p.Phe556Tyr
ENST00000649884.1:c.1448T>A ENSP00000497040.1:p.Phe483Tyr
ENST00000239587.9:c.1667T>A ENSP00000239587.5:p.Phe556Tyr
ENST00000515138.1:c.1667T>A ENSP00000424130.1:p.Phe556Tyr
NM_031949.4:c.1667T>A NP_114155.4:p.Phe556Tyr
XM_006715572.2:c.1448T>A XP_006715635.1:p.Phe483Tyr
XM_006715572.4:c.1448T>A XP_006715635.1:p.Phe483Tyr
NM_031949.5:c.1667T>A MANE Select NP_114155.4:p.Phe556Tyr
Search 100 bp 5'
Search 100 bp 3'