Canonical Allele Identifier: CA309356163
Gene: FUT1 HGNC NCBI

Linked Data

dbSNP Id: rs838143
MyVariant Identifiers: chr19:g.48748498G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48748498G>C , CM000681.2:g.48748498G>C GRCh38
NC_000019.9:g.49251755G>C , CM000681.1:g.49251755G>C GRCh37
NC_000019.8:g.53943567G>C NCBI36
NG_007510.1:g.11893C>G
NG_007510.2:g.11893C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645652.2:c.*1686C>G MANE Select ENSP00000494643.1:n.*1686C>G
ENST00000310160.7:c.*1686C>G ENSP00000312021.3:n.*1686C>G
NM_000148.3:c.*1686C>G NP_000139.1:n.*1686C>G
XM_006723127.1:c.*1686C>G XP_006723190.1:n.*1686C>G
NM_001329877.1:c.*1686C>G NP_001316806.1:n.*1686C>G
NM_000148.4:c.*1686C>G NP_000139.1:n.*1686C>G
NM_001384359.1:c.*1686C>G MANE Select NP_001371288.1:n.*1686C>G
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