Canonical Allele Identifier: CA1172961675
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1667515020
gnomAD v3: 1-67009216-C-T
gnomAD v4: 1-67009216-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009216C>T , CM000663.2:g.67009216C>T GRCh38
NC_000001.10:g.67474899C>T , CM000663.1:g.67474899C>T GRCh37
NC_000001.9:g.67247487C>T NCBI36
NG_012933.1:g.50182G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-49G>A MANE Select ENSP00000235345.5:n.877-49G>A
ENST00000235345.5:c.877-49G>A ENSP00000235345.5:n.877-49G>A
NM_015139.2:c.877-49G>A NP_055954.1:n.877-49G>A
XM_006710478.1:c.958-49G>A XP_006710541.1:n.958-49G>A
XM_011541070.1:c.958-49G>A XP_011539372.1:n.958-49G>A
XM_006710478.2:c.958-49G>A XP_006710541.1:n.958-49G>A
XM_011541070.2:c.958-49G>A XP_011539372.1:n.958-49G>A
XR_001737057.2:n.1461-49G>A
XR_001737058.2:n.2246-49G>A
NM_015139.3:c.877-49G>A MANE Select NP_055954.1:n.877-49G>A