Canonical Allele Identifier: CA463520085

Gene: FAM83H

Linked Data

• dbSNP Id: rs1818401260
• gnomAD v4: 8-143728633-G-A
• MyVariant Identifiers: chr8:g.144810803G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728633G>A , CM000670.2:g.143728633G>A	GRCh38
NC_000008.10:g.144810803G>A , CM000670.1:g.144810803G>A	GRCh37
NC_000008.9:g.144882791G>A	NCBI36
NG_016652.1:g.10112C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.828C>T MANE Select	ENSP00000373565.3:p.Ile276=
ENST00000650760.1:c.1431C>T	ENSP00000499217.1:p.Ile477=
ENST00000388913.3:c.828C>T	ENSP00000373565.3:p.Ile276=
ENST00000395103.2:c.8C>T
NM_198488.3:c.828C>T	NP_940890.3:p.Ile276=
XM_005250887.2:c.885C>T	XP_005250944.1:p.Ile295=
XM_005250888.2:c.846C>T	XP_005250945.1:p.Ile282=
XM_005250889.2:c.828C>T	XP_005250946.1:p.Ile276=
XM_011516980.1:c.1149C>T	XP_011515282.1:p.Ile383=
XM_011516981.1:c.996C>T	XP_011515283.1:p.Ile332=
XM_005250887.3:c.885C>T	XP_005250944.1:p.Ile295=
XM_005250888.3:c.846C>T	XP_005250945.1:p.Ile282=
XM_005250889.3:c.828C>T	XP_005250946.1:p.Ile276=
XM_011516980.2:c.1431C>T	XP_011515282.2:p.Ile477=
XM_011516981.2:c.996C>T	XP_011515283.1:p.Ile332=
XM_024447131.1:c.828C>T	XP_024302899.1:p.Ile276=
NM_198488.4:c.828C>T	NP_940890.3:p.Ile276=
NM_198488.5:c.828C>T MANE Select	NP_940890.4:p.Ile276=