Canonical Allele Identifier: CA15955168
Gene: FUT1 HGNC NCBI

Linked Data

dbSNP Id: rs838143
gnomAD v2: 19-49251755-G-A
gnomAD v3: 19-48748498-G-A
gnomAD v4: 19-48748498-G-A
MyVariant Identifiers: chr19:g.49251755G>A (hg19) chr19:g.48748498G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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