Canonical Allele Identifier: CA1504952814
Gene: FGG HGNC NCBI

Linked Data

dbSNP Id: rs2066861
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154606284C>G , CM000666.2:g.154606284C>G GRCh38
NC_000004.11:g.155527436C>G , CM000666.1:g.155527436C>G GRCh37
NC_000004.10:g.155746886C>G NCBI36
NG_008834.1:g.11467G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336098.8:c.1129+421G>C MANE Select ENSP00000336829.3:n.1129+421G>C
ENST00000336098.7:c.1129+421G>C ENSP00000336829.3:n.1129+421G>C
ENST00000404648.7:c.1129+421G>C ENSP00000384860.3:n.1129+421G>C
ENST00000405164.5:c.1153+421G>C ENSP00000384101.1:n.1153+421G>C
ENST00000407946.5:c.1153+421G>C ENSP00000384552.1:n.1153+421G>C
ENST00000465913.1:n.677+421G>C
ENST00000492082.5:n.1671+421G>C
NM_000509.4:c.1129+421G>C NP_000500.2:n.1129+421G>C
NM_000509.5:c.1129+421G>C NP_000500.2:n.1129+421G>C
NM_021870.2:c.1129+421G>C NP_068656.2:n.1129+421G>C
NM_021870.3:c.1129+421G>C MANE Select NP_068656.2:n.1129+421G>C
NM_000509.6:c.1129+421G>C NP_000500.2:n.1129+421G>C
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