Canonical Allele Identifier: CA372469322

Gene: FAM83H

Linked Data

• dbSNP Id: rs1554623524
• gnomAD v2: 8-144810769-C-T
• gnomAD v4: 8-143728599-C-T
• MyVariant Identifiers: chr8:g.144810769C>T (hg19) ; chr8:g.143728599C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728599C>T , CM000670.2:g.143728599C>T	GRCh38
NC_000008.10:g.144810769C>T , CM000670.1:g.144810769C>T	GRCh37
NC_000008.9:g.144882757C>T	NCBI36
NG_016652.1:g.10146G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.862G>A MANE Select	ENSP00000373565.3:p.Ala288Thr
ENST00000650760.1:c.1465G>A	ENSP00000499217.1:p.Ala489Thr
ENST00000388913.3:c.862G>A	ENSP00000373565.3:p.Ala288Thr
ENST00000395103.2:c.42G>A
NM_198488.3:c.862G>A	NP_940890.3:p.Ala288Thr
XM_005250887.2:c.919G>A	XP_005250944.1:p.Ala307Thr
XM_005250888.2:c.880G>A	XP_005250945.1:p.Ala294Thr
XM_005250889.2:c.862G>A	XP_005250946.1:p.Ala288Thr
XM_011516980.1:c.1183G>A	XP_011515282.1:p.Ala395Thr
XM_011516981.1:c.1030G>A	XP_011515283.1:p.Ala344Thr
XM_005250887.3:c.919G>A	XP_005250944.1:p.Ala307Thr
XM_005250888.3:c.880G>A	XP_005250945.1:p.Ala294Thr
XM_005250889.3:c.862G>A	XP_005250946.1:p.Ala288Thr
XM_011516980.2:c.1465G>A	XP_011515282.2:p.Ala489Thr
XM_011516981.2:c.1030G>A	XP_011515283.1:p.Ala344Thr
XM_024447131.1:c.862G>A	XP_024302899.1:p.Ala288Thr
NM_198488.4:c.862G>A	NP_940890.3:p.Ala288Thr
NM_198488.5:c.862G>A MANE Select	NP_940890.4:p.Ala288Thr