Canonical Allele Identifier: CA144124241
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs904015307
MyVariant Identifiers: chr6:g.96505304A>G (hg19) chr6:g.96057428A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057428A>G , CM000668.2:g.96057428A>G GRCh38
NC_000006.11:g.96505304A>G , CM000668.1:g.96505304A>G GRCh37
NC_000006.10:g.96612025A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302103.6:c.-98+41216A>G MANE Select ENSP00000302599.4:n.-98+41216A>G
ENST00000302103.5:c.-98+41216A>G ENSP00000302599.4:n.-98+41216A>G
NM_006581.3:c.-98+41216A>G NP_006572.2:n.-98+41216A>G
XM_011535384.1:c.-98+36455A>G XP_011533686.1:n.-98+36455A>G
XM_017010190.1:c.-215+41216A>G XP_016865679.1:n.-215+41216A>G
XR_001744267.2:n.1830T>C
NM_006581.4:c.-98+41216A>G MANE Select NP_006572.2:n.-98+41216A>G
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