Canonical Allele Identifier: CA817831249

Gene: SLC35F1

Linked Data

• dbSNP Id: rs1422482636
• gnomAD v3: 6-118297732-G-T
• gnomAD v4: 6-118297732-G-T
• MyVariant Identifiers: chr6:g.118618895G>T (hg19) ; chr6:g.118297732G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118297732G>T , CM000668.2:g.118297732G>T	GRCh38
NC_000006.11:g.118618895G>T , CM000668.1:g.118618895G>T	GRCh37
NC_000006.10:g.118725588G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360388.9:c.1002+12394G>T MANE Select	ENSP00000353557.4:n.1002+12394G>T
ENST00000360388.8:c.1002+12394G>T	ENSP00000353557.4:n.1002+12394G>T
ENST00000621341.1:c.825+12394G>T	ENSP00000484738.1:n.825+12394G>T
NM_001029858.3:c.1002+12394G>T	NP_001025029.2:n.1002+12394G>T
XM_005266865.3:c.1002+12394G>T	XP_005266922.1:n.1002+12394G>T
XR_942913.1:n.342-7222C>A
XM_005266865.4:c.1002+12394G>T	XP_005266922.1:n.1002+12394G>T
NM_001029858.4:c.1002+12394G>T MANE Select	NP_001025029.2:n.1002+12394G>T