Canonical Allele Identifier: CA4097490

Gene: TTLL2

Linked Data

• dbSNP Id: rs779289472
• ExAC: 6:167754585 A / G
• gnomAD v2: 6-167754585-A-G
• MyVariant Identifiers: chr6:g.167754585A>G (hg19) ; chr6:g.167341097A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167341097A>G , CM000668.2:g.167341097A>G	GRCh38
NC_000006.11:g.167754585A>G , CM000668.1:g.167754585A>G	GRCh37
NC_000006.10:g.167674575A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239587.10:c.1197A>G MANE Select	ENSP00000239587.5:p.Thr399=
ENST00000649884.1:c.978A>G	ENSP00000497040.1:p.Thr326=
ENST00000239587.9:c.1197A>G	ENSP00000239587.5:p.Thr399=
ENST00000515138.1:c.1197A>G	ENSP00000424130.1:p.Thr399=
NM_031949.4:c.1197A>G	NP_114155.4:p.Thr399=
XM_006715572.2:c.978A>G	XP_006715635.1:p.Thr326=
XM_006715572.4:c.978A>G	XP_006715635.1:p.Thr326=
NM_031949.5:c.1197A>G MANE Select	NP_114155.4:p.Thr399=