Canonical Allele Identifier: CA344670224

Gene: FAM177B

Linked Data

• MyVariant Identifiers: chr1:g.222923360G>C (hg19) ; chr1:g.222750018G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222750018G>C , CM000663.2:g.222750018G>C	GRCh38
NC_000001.10:g.222923360G>C , CM000663.1:g.222923360G>C	GRCh37
NC_000001.9:g.220989983G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000445590.4:c.437G>C MANE Select	ENSP00000414451.2:p.Gly146Ala
ENST00000360827.6:c.437G>C	ENSP00000354070.2:p.Gly146Ala
ENST00000391880.6:c.*578G>C	ENSP00000375752.2:n.*578G>C
ENST00000445590.3:c.437G>C	ENSP00000414451.2:p.Gly146Ala
NM_207468.2:c.437G>C	NP_997351.2:p.Gly146Ala
XM_006711318.2:c.241+2937G>C	XP_006711381.1:n.241+2937G>C
NM_001324080.1:c.437G>C	NP_001311009.1:p.Gly146Ala
NR_136691.1:n.1207G>C
XM_017001279.1:c.437G>C	XP_016856768.1:p.Gly146Ala
XM_017001280.1:c.437G>C	XP_016856769.1:p.Gly146Ala
XM_017001281.1:c.437G>C	XP_016856770.1:p.Gly146Ala
XM_017001282.1:c.437G>C	XP_016856771.1:p.Gly146Ala
XM_017001285.1:c.274+2937G>C	XP_016856774.1:n.274+2937G>C
NM_001324080.2:c.437G>C	NP_001311009.1:p.Gly146Ala
NM_207468.3:c.437G>C	NP_997351.2:p.Gly146Ala
NR_136691.2:n.1221G>C
NM_001394345.1:c.437G>C MANE Select	NP_001381274.1:p.Gly146Ala