Canonical Allele Identifier: CA508272200

Gene: FUT2

Linked Data

• dbSNP Id: rs1180351197
• gnomAD v3: 19-48703571-T-C
• gnomAD v4: 19-48703571-T-C
• MyVariant Identifiers: chr19:g.49206828T>C (hg19) ; chr19:g.48703571T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703571T>C , CM000681.2:g.48703571T>C	GRCh38
NC_000019.9:g.49206828T>C , CM000681.1:g.49206828T>C	GRCh37
NC_000019.8:g.53898640T>C	NCBI36
NG_007511.1:g.12601T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000425340.3:c.615T>C MANE Select	ENSP00000387498.2:p.Tyr205=
ENST00000522966.2:c.615T>C	ENSP00000430227.2:p.Tyr205=
ENST00000391876.5:c.615T>C	ENSP00000375748.4:p.Tyr205=
ENST00000425340.2:c.615T>C	ENSP00000387498.2:p.Tyr205=
ENST00000522966.1:c.615T>C	ENSP00000430227.1:p.Tyr205=
NM_000511.5:c.615T>C	NP_000502.4:p.Tyr205=
NM_001097638.2:c.615T>C	NP_001091107.1:p.Tyr205=
NR_131188.1:n.278A>G
NM_000511.6:c.615T>C MANE Select	NP_000502.4:p.Tyr205=
NM_001097638.3:c.615T>C	NP_001091107.1:p.Tyr205=