Canonical Allele Identifier: CA738095417
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1357000910
MyVariant Identifiers: chr1:g.67475083G>T (hg19) chr1:g.67009400G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009400G>T , CM000663.2:g.67009400G>T GRCh38
NC_000001.10:g.67475083G>T , CM000663.1:g.67475083G>T GRCh37
NC_000001.9:g.67247671G>T NCBI36
NG_012933.1:g.49998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-233C>A MANE Select ENSP00000235345.5:n.877-233C>A
ENST00000235345.5:c.877-233C>A ENSP00000235345.5:n.877-233C>A
NM_015139.2:c.877-233C>A NP_055954.1:n.877-233C>A
XM_006710478.1:c.958-233C>A XP_006710541.1:n.958-233C>A
XM_011541070.1:c.958-233C>A XP_011539372.1:n.958-233C>A
XM_006710478.2:c.958-233C>A XP_006710541.1:n.958-233C>A
XM_011541070.2:c.958-233C>A XP_011539372.1:n.958-233C>A
XR_001737057.2:n.1461-233C>A
XR_001737058.2:n.2246-233C>A
NM_015139.3:c.877-233C>A MANE Select NP_055954.1:n.877-233C>A
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