Canonical Allele Identifier: CA349632859

Gene: SLC25A12

Linked Data

• dbSNP Id: rs1685036227
• gnomAD v4: 2-171855939-A-G
• MyVariant Identifiers: chr2:g.172712449A>G (hg19) ; chr2:g.171855939A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171855939A>G , CM000664.2:g.171855939A>G	GRCh38
NC_000002.11:g.172712449A>G , CM000664.1:g.172712449A>G	GRCh37
NC_000002.10:g.172420695A>G	NCBI36
NG_011781.1:g.43365T>C
NG_011781.2:g.43365T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422440.7:c.220T>C MANE Select	ENSP00000388658.2:p.Tyr74His
ENST00000263812.8:c.210-11431T>C	ENSP00000263812.4:n.210-11431T>C
ENST00000422440.6:c.220T>C	ENSP00000388658.2:p.Tyr74His
ENST00000426896.5:c.220T>C	ENSP00000413968.1:p.Tyr74His
ENST00000464063.1:n.541T>C
ENST00000472748.5:n.385T>C
ENST00000475360.6:c.208T>C	ENSP00000437845.1:p.Tyr70His
ENST00000484227.5:n.418T>C
NM_003705.4:c.220T>C	NP_003696.2:p.Tyr74His
NR_047549.1:n.302-11431T>C
XM_005246923.3:c.169T>C	XP_005246980.1:p.Tyr57His
XM_011512069.1:c.220T>C	XP_011510371.1:p.Tyr74His
XM_011512070.1:c.-158T>C	XP_011510372.1:n.-158T>C
XM_011512070.3:c.-158T>C	XP_011510372.1:n.-158T>C
NM_003705.5:c.220T>C MANE Select	NP_003696.2:p.Tyr74His
NR_047549.2:n.240-11431T>C