Canonical Allele Identifier: CA406713386
Gene: FUT2 HGNC NCBI

Linked Data

gnomAD v4: 19-48703919-G-T
MyVariant Identifiers: chr19:g.49207176G>T (hg19) chr19:g.48703919G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703919G>T , CM000681.2:g.48703919G>T GRCh38
NC_000019.9:g.49207176G>T , CM000681.1:g.49207176G>T GRCh37
NC_000019.8:g.53898988G>T NCBI36
NG_007511.1:g.12949G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.963G>T MANE Select ENSP00000387498.2:p.Lys321Asn
ENST00000522966.2:c.963G>T ENSP00000430227.2:p.Lys321Asn
ENST00000391876.5:c.963G>T ENSP00000375748.4:p.Lys321Asn
ENST00000425340.2:c.963G>T ENSP00000387498.2:p.Lys321Asn
NM_000511.5:c.963G>T NP_000502.4:p.Lys321Asn
NM_001097638.2:c.963G>T NP_001091107.1:p.Lys321Asn
NM_000511.6:c.963G>T MANE Select NP_000502.4:p.Lys321Asn
NM_001097638.3:c.963G>T NP_001091107.1:p.Lys321Asn
Search 100 bp 5'
Search 100 bp 3'