Canonical Allele Identifier: CA899211

Gene: SLC35D1

Linked Data

• dbSNP Id: rs201110844
• ExAC: 1:67519714 T / C
• gnomAD v2: 1-67519714-T-C
• gnomAD v3: 1-67054031-T-C
• gnomAD v4: 1-67054031-T-C
• MyVariant Identifiers: chr1:g.67519714T>C (hg19) ; chr1:g.67054031T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054031T>C , CM000663.2:g.67054031T>C	GRCh38
NC_000001.10:g.67519714T>C , CM000663.1:g.67519714T>C	GRCh37
NC_000001.9:g.67292302T>C	NCBI36
NG_012933.1:g.5367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.-18A>G MANE Select	ENSP00000235345.5:n.-18A>G
ENST00000235345.5:c.-18A>G	ENSP00000235345.5:n.-18A>G
NM_015139.2:c.-18A>G	NP_055954.1:n.-18A>G
XM_006710478.1:c.-18A>G	XP_006710541.1:n.-18A>G
XM_011541070.1:c.-18A>G	XP_011539372.1:n.-18A>G
XM_006710478.2:c.-18A>G	XP_006710541.1:n.-18A>G
XM_011541070.2:c.-18A>G	XP_011539372.1:n.-18A>G
XR_001737057.2:n.393A>G
XR_001737058.2:n.386A>G
NM_015139.3:c.-18A>G MANE Select	NP_055954.1:n.-18A>G