Canonical Allele Identifier: CA406710389

Gene: FUT2

Linked Data

• MyVariant Identifiers: chr19:g.49206655A>C (hg19) ; chr19:g.48703398A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703398A>C , CM000681.2:g.48703398A>C	GRCh38
NC_000019.9:g.49206655A>C , CM000681.1:g.49206655A>C	GRCh37
NC_000019.8:g.53898467A>C	NCBI36
NG_007511.1:g.12428A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.442A>C MANE Select	ENSP00000387498.2:p.Thr148Pro
ENST00000522966.2:c.442A>C	ENSP00000430227.2:p.Thr148Pro
ENST00000391876.5:c.442A>C	ENSP00000375748.4:p.Thr148Pro
ENST00000425340.2:c.442A>C	ENSP00000387498.2:p.Thr148Pro
ENST00000522966.1:c.442A>C	ENSP00000430227.1:p.Thr148Pro
NM_000511.5:c.442A>C	NP_000502.4:p.Thr148Pro
NM_001097638.2:c.442A>C	NP_001091107.1:p.Thr148Pro
NR_131188.1:n.451T>G
NM_000511.6:c.442A>C MANE Select	NP_000502.4:p.Thr148Pro
NM_001097638.3:c.442A>C	NP_001091107.1:p.Thr148Pro