Canonical Allele Identifier: CA358538576

Gene: FGG

Linked Data

• dbSNP Id: rs1163362139
• gnomAD v3: 4-154612434-T-C
• gnomAD v4: 4-154612434-T-C
• MyVariant Identifiers: chr4:g.155533586T>C (hg19) ; chr4:g.154612434T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154612434T>C , CM000666.2:g.154612434T>C	GRCh38
NC_000004.11:g.155533586T>C , CM000666.1:g.155533586T>C	GRCh37
NC_000004.10:g.155753036T>C	NCBI36
NG_008834.1:g.5317A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.80A>G MANE Select	ENSP00000336829.3:p.Tyr27Cys
ENST00000336098.7:c.80A>G	ENSP00000336829.3:p.Tyr27Cys
ENST00000393846.6:c.-230A>G	ENSP00000377429.2:n.-230A>G
ENST00000404648.7:c.80A>G	ENSP00000384860.3:p.Tyr27Cys
ENST00000405164.5:c.80A>G	ENSP00000384101.1:p.Tyr27Cys
ENST00000407946.5:c.80A>G	ENSP00000384552.1:p.Tyr27Cys
ENST00000443553.5:c.-196A>G	ENSP00000407562.1:n.-196A>G
ENST00000464532.5:n.127A>G
ENST00000465336.1:n.127A>G
ENST00000473393.5:n.106A>G
ENST00000484695.1:n.82A>G
ENST00000492082.5:n.130A>G
NM_000509.4:c.80A>G	NP_000500.2:p.Tyr27Cys
NM_000509.5:c.80A>G	NP_000500.2:p.Tyr27Cys
NM_021870.2:c.80A>G	NP_068656.2:p.Tyr27Cys
NM_021870.3:c.80A>G MANE Select	NP_068656.2:p.Tyr27Cys
NM_000509.6:c.80A>G	NP_000500.2:p.Tyr27Cys