Canonical Allele Identifier: CA406703112
Gene: FUT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49254096T>C (hg19) chr19:g.48750839T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48750839T>C , CM000681.2:g.48750839T>C GRCh38
NC_000019.9:g.49254096T>C , CM000681.1:g.49254096T>C GRCh37
NC_000019.8:g.53945908T>C NCBI36
NG_007510.1:g.9552A>G
NG_007510.2:g.9552A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645652.2:c.443A>G MANE Select ENSP00000494643.1:p.Asp148Gly
ENST00000310160.7:c.443A>G ENSP00000312021.3:p.Asp148Gly
NM_000148.3:c.443A>G NP_000139.1:p.Asp148Gly
XM_006723127.1:c.812A>G XP_006723190.1:p.Asp271Gly
NM_001329877.1:c.443A>G NP_001316806.1:p.Asp148Gly
NM_000148.4:c.443A>G NP_000139.1:p.Asp148Gly
NM_001384359.1:c.443A>G MANE Select NP_001371288.1:p.Asp148Gly
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