Canonical Allele Identifier: CA3114712

Gene: FGB

Linked Data

• dbSNP Id: rs764656753
• ExAC: 4:155490772 C / CCAAAAATAAAATTT
• MyVariant Identifiers: chr4:g.155490772_155490773insCAAAAATAAAATTT (hg19) ; chr4:g.154569620_154569621insCAAAAATAAAATTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569620_154569621insCAAAAATAAAATTT , CM000666.2:g.154569620_154569621insCAAAAATAAAATTT	GRCh38
NC_000004.11:g.155490772_155490773insCAAAAATAAAATTT , CM000666.1:g.155490772_155490773insCAAAAATAAAATTT	GRCh37
NC_000004.10:g.155710222_155710223insCAAAAATAAAATTT	NCBI36
NG_008833.1:g.11641_11642insCAAAAATAAAATTT , LRG_558:g.11641_11642insCAAAAATAAAATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1065_1066insCAAAAATAAAATTT MANE Select	ENSP00000306099.4:p.Tyr356GlnfsTer3
ENST00000302068.8:c.1065_1066insCAAAAATAAAATTT	ENSP00000306099.4:p.Tyr356GlnfsTer3
ENST00000502545.5:n.939+313_939+314insCAAAAATAAAATTT
ENST00000509493.1:c.408_409insCAAAAATAAAATTT	ENSP00000426757.1:p.Tyr137GlnfsTer3
NM_001184741.1:c.888_889insCAAAAATAAAATTT	NP_001171670.1:p.Tyr297GlnfsTer3
NM_005141.4:c.1065_1066insCAAAAATAAAATTT , LRG_558t1:c.1065_1066insCAAAAATAAAATTT	NP_005132.2:p.Tyr356GlnfsTer3
NM_001382759.1:c.933_934insCAAAAATAAAATTT	NP_001369688.1:p.Tyr312GlnfsTer3
NM_001382760.1:c.1065_1066insCAAAAATAAAATTT	NP_001369689.1:p.Tyr356GlnfsTer3
NM_001382761.1:c.1065_1066insCAAAAATAAAATTT	NP_001369690.1:p.Tyr356GlnfsTer3
NM_001382762.1:c.765_766insCAAAAATAAAATTT	NP_001369691.1:p.Tyr256GlnfsTer3
NM_001382763.1:c.1056_1057insCAAAAATAAAATTT	NP_001369692.1:p.Tyr353GlnfsTer3
NM_001382764.1:c.1065_1066insCAAAAATAAAATTT	NP_001369693.1:p.Tyr356GlnfsTer3
NM_001382765.1:c.1065_1066insCAAAAATAAAATTT	NP_001369694.1:p.Tyr356GlnfsTer3
NM_005141.5:c.1065_1066insCAAAAATAAAATTT MANE Select	NP_005132.2:p.Tyr356GlnfsTer3