Canonical Allele Identifier: CA2702736729

Gene: KLHDC8B

Linked Data

• dbSNP Id: rs2107658584

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49173310T>A , CM000665.2:g.49173310T>A	GRCh38
NC_000003.11:g.49210743T>A , CM000665.1:g.49210743T>A	GRCh37
NC_000003.10:g.49185747T>A	NCBI36
NG_027702.1:g.6726T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332780.4:c.376+165T>A MANE Select	ENSP00000327468.2:n.376+165T>A
ENST00000332780.3:c.376+165T>A	ENSP00000327468.2:n.376+165T>A
ENST00000459846.6:n.230+509T>A
ENST00000476495.2:n.463+135T>A
NM_173546.2:c.376+165T>A	NP_775817.1:n.376+165T>A
XM_005264938.1:c.376+165T>A	XP_005264995.1:n.376+165T>A
XM_005264939.3:c.-6+509T>A	XP_005264996.1:n.-6+509T>A
XM_005264940.3:c.-6+509T>A	XP_005264997.1:n.-6+509T>A
XM_006713015.1:c.406+135T>A	XP_006713078.1:n.406+135T>A
XM_006713016.1:c.406+135T>A	XP_006713079.1:n.406+135T>A
XM_005264938.3:c.376+165T>A	XP_005264995.1:n.376+165T>A
XM_005264940.4:c.-6+509T>A	XP_005264997.1:n.-6+509T>A
XM_006713015.3:c.406+135T>A	XP_006713078.1:n.406+135T>A
XM_006713016.3:c.406+135T>A	XP_006713079.1:n.406+135T>A
NM_173546.3:c.376+165T>A MANE Select	NP_775817.1:n.376+165T>A