Canonical Allele Identifier: CA372468854

Gene: FAM83H

Linked Data

• gnomAD v4: 8-143728446-C-G
• MyVariant Identifiers: chr8:g.144810616C>G (hg19) ; chr8:g.143728446C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728446C>G , CM000670.2:g.143728446C>G	GRCh38
NC_000008.10:g.144810616C>G , CM000670.1:g.144810616C>G	GRCh37
NC_000008.9:g.144882604C>G	NCBI36
NG_016652.1:g.10299G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.1015G>C MANE Select	ENSP00000373565.3:p.Gly339Arg
ENST00000650760.1:c.1618G>C	ENSP00000499217.1:p.Gly540Arg
ENST00000388913.3:c.1015G>C	ENSP00000373565.3:p.Gly339Arg
ENST00000395103.2:c.195G>C
NM_198488.3:c.1015G>C	NP_940890.3:p.Gly339Arg
XM_005250887.2:c.1072G>C	XP_005250944.1:p.Gly358Arg
XM_005250888.2:c.1033G>C	XP_005250945.1:p.Gly345Arg
XM_005250889.2:c.1015G>C	XP_005250946.1:p.Gly339Arg
XM_011516980.1:c.1336G>C	XP_011515282.1:p.Gly446Arg
XM_011516981.1:c.1183G>C	XP_011515283.1:p.Gly395Arg
XM_005250887.3:c.1072G>C	XP_005250944.1:p.Gly358Arg
XM_005250888.3:c.1033G>C	XP_005250945.1:p.Gly345Arg
XM_005250889.3:c.1015G>C	XP_005250946.1:p.Gly339Arg
XM_011516980.2:c.1618G>C	XP_011515282.2:p.Gly540Arg
XM_011516981.2:c.1183G>C	XP_011515283.1:p.Gly395Arg
XM_024447131.1:c.1015G>C	XP_024302899.1:p.Gly339Arg
NM_198488.4:c.1015G>C	NP_940890.3:p.Gly339Arg
NM_198488.5:c.1015G>C MANE Select	NP_940890.4:p.Gly339Arg