Canonical Allele Identifier: CA2646115966
Gene: SLC35D1 HGNC NCBI

Linked Data

gnomAD v4: 1-67009036-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009036T>C , CM000663.2:g.67009036T>C GRCh38
NC_000001.10:g.67474719T>C , CM000663.1:g.67474719T>C GRCh37
NC_000001.9:g.67247307T>C NCBI36
NG_012933.1:g.50362A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.959+49A>G MANE Select ENSP00000235345.5:n.959+49A>G
ENST00000235345.5:c.959+49A>G ENSP00000235345.5:n.959+49A>G
NM_015139.2:c.959+49A>G NP_055954.1:n.959+49A>G
XM_006710478.1:c.1040+49A>G XP_006710541.1:n.1040+49A>G
XM_011541070.1:c.1040+49A>G XP_011539372.1:n.1040+49A>G
XM_006710478.2:c.1040+49A>G XP_006710541.1:n.1040+49A>G
XM_011541070.2:c.1040+49A>G XP_011539372.1:n.1040+49A>G
XR_001737057.2:n.1543+49A>G
XR_001737058.2:n.2328+49A>G
NM_015139.3:c.959+49A>G MANE Select NP_055954.1:n.959+49A>G