Canonical Allele Identifier: CA899799105

Gene: SLC25A36

Linked Data

• dbSNP Id: rs1378180518
• gnomAD v3: 3-140957858-C-G
• gnomAD v4: 3-140957858-C-G
• MyVariant Identifiers: chr3:g.140676700C>G (hg19) ; chr3:g.140957858C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140957858C>G , CM000665.2:g.140957858C>G	GRCh38
NC_000003.11:g.140676700C>G , CM000665.1:g.140676700C>G	GRCh37
NC_000003.10:g.142159390C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000324194.12:c.206+1167C>G MANE Select	ENSP00000320688.6:n.206+1167C>G
ENST00000648615.1:c.206+1167C>G	ENSP00000497436.1:n.206+1167C>G
ENST00000324194.10:c.206+1167C>G	ENSP00000320688.6:n.206+1167C>G
ENST00000393015.8:n.408+1167C>G
ENST00000446041.6:c.206+1167C>G	ENSP00000401938.2:n.206+1167C>G
ENST00000453248.6:c.206+1167C>G	ENSP00000391521.2:n.206+1167C>G
ENST00000502594.5:c.206+1167C>G	ENSP00000423319.1:n.206+1167C>G
ENST00000507429.5:c.206+1167C>G	ENSP00000421470.1:n.206+1167C>G
ENST00000512023.5:c.56+1167C>G	ENSP00000424505.1:n.56+1167C>G
ENST00000512506.5:c.56+1167C>G	ENSP00000423711.1:n.56+1167C>G
ENST00000513887.5:c.56+1167C>G	ENSP00000422265.1:n.56+1167C>G
ENST00000515813.1:n.393+1167C>G
ENST00000631654.1:c.206+1167C>G	ENSP00000487839.1:n.206+1167C>G
NM_001104647.1:c.206+1167C>G	NP_001098117.1:n.206+1167C>G
NM_018155.2:c.206+1167C>G	NP_060625.2:n.206+1167C>G
XM_011512951.1:c.302+1167C>G	XP_011511253.1:n.302+1167C>G
XM_011512953.1:c.302+1167C>G	XP_011511255.1:n.302+1167C>G
XR_924150.1:n.495+1167C>G
XR_924151.1:n.495+1167C>G
XR_924152.1:n.495+1167C>G
XR_924153.1:n.495+1167C>G
XR_924154.1:n.495+1167C>G
XR_924155.1:n.495+1167C>G
XR_924156.1:n.495+1167C>G
XR_924157.1:n.495+1167C>G
NM_001104647.3:c.206+1167C>G MANE Select	NP_001098117.1:n.206+1167C>G
NM_018155.3:c.206+1167C>G	NP_060625.2:n.206+1167C>G