Canonical Allele Identifier: CA1093644709
Gene: SLC35F1 HGNC NCBI

Linked Data

dbSNP Id: rs1776208938
gnomAD v3: 6-118297726-A-G
gnomAD v4: 6-118297726-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.118297726A>G , CM000668.2:g.118297726A>G GRCh38
NC_000006.11:g.118618889A>G , CM000668.1:g.118618889A>G GRCh37
NC_000006.10:g.118725582A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360388.9:c.1002+12388A>G MANE Select ENSP00000353557.4:n.1002+12388A>G
ENST00000360388.8:c.1002+12388A>G ENSP00000353557.4:n.1002+12388A>G
ENST00000621341.1:c.825+12388A>G ENSP00000484738.1:n.825+12388A>G
NM_001029858.3:c.1002+12388A>G NP_001025029.2:n.1002+12388A>G
XM_005266865.3:c.1002+12388A>G XP_005266922.1:n.1002+12388A>G
XR_942913.1:n.342-7216T>C
XM_005266865.4:c.1002+12388A>G XP_005266922.1:n.1002+12388A>G
NM_001029858.4:c.1002+12388A>G MANE Select NP_001025029.2:n.1002+12388A>G
Search 100 bp 5'
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