Canonical Allele Identifier: CA372469015

Gene: FAM83H

Linked Data

• dbSNP Id: rs1554623470
• gnomAD v2: 8-144810684-G-A
• gnomAD v4: 8-143728514-G-A
• MyVariant Identifiers: chr8:g.144810684G>A (hg19) ; chr8:g.143728514G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728514G>A , CM000670.2:g.143728514G>A	GRCh38
NC_000008.10:g.144810684G>A , CM000670.1:g.144810684G>A	GRCh37
NC_000008.9:g.144882672G>A	NCBI36
NG_016652.1:g.10231C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.947C>T MANE Select	ENSP00000373565.3:p.Ala316Val
ENST00000650760.1:c.1550C>T	ENSP00000499217.1:p.Ala517Val
ENST00000388913.3:c.947C>T	ENSP00000373565.3:p.Ala316Val
ENST00000395103.2:c.127C>T
NM_198488.3:c.947C>T	NP_940890.3:p.Ala316Val
XM_005250887.2:c.1004C>T	XP_005250944.1:p.Ala335Val
XM_005250888.2:c.965C>T	XP_005250945.1:p.Ala322Val
XM_005250889.2:c.947C>T	XP_005250946.1:p.Ala316Val
XM_011516980.1:c.1268C>T	XP_011515282.1:p.Ala423Val
XM_011516981.1:c.1115C>T	XP_011515283.1:p.Ala372Val
XM_005250887.3:c.1004C>T	XP_005250944.1:p.Ala335Val
XM_005250888.3:c.965C>T	XP_005250945.1:p.Ala322Val
XM_005250889.3:c.947C>T	XP_005250946.1:p.Ala316Val
XM_011516980.2:c.1550C>T	XP_011515282.2:p.Ala517Val
XM_011516981.2:c.1115C>T	XP_011515283.1:p.Ala372Val
XM_024447131.1:c.947C>T	XP_024302899.1:p.Ala316Val
NM_198488.4:c.947C>T	NP_940890.3:p.Ala316Val
NM_198488.5:c.947C>T MANE Select	NP_940890.4:p.Ala316Val