Canonical Allele Identifier: CA150786

Gene: FAM111B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.59125976A>G , CM000673.2:g.59125976A>G	GRCh38
NC_000011.9:g.58893449A>G , CM000673.1:g.58893449A>G	GRCh37
NC_000011.8:g.58650025A>G	NCBI36
NG_034129.1:g.23792A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_198947.4:c.1879A>G MANE Select	NP_945185.1:p.Arg627Gly
ENST00000343597.4:c.1879A>G MANE Select	ENSP00000341565.3:p.Arg627Gly
NM_001142703.1:c.1789A>G	NP_001136175.1:p.Arg597Gly
NM_001142703.2:c.1789A>G	NP_001136175.1:p.Arg597Gly
NM_001142704.1:c.1789A>G	NP_001136176.1:p.Arg597Gly
NM_001142704.2:c.1789A>G	NP_001136176.1:p.Arg597Gly
NM_198947.3:c.1879A>G	NP_945185.1:p.Arg627Gly
ENST00000343597.3:c.1879A>G	ENSP00000341565.3:p.Arg627Gly
ENST00000411426.1:c.1789A>G	ENSP00000393855.1:p.Arg597Gly
ENST00000529618.5:c.1789A>G	ENSP00000432875.1:p.Arg597Gly
ENST00000620384.1:c.1879A>G	ENSP00000483456.1:p.Arg627Gly