Canonical Allele Identifier: CA779677852

Gene: SLC14A2

Linked Data

• dbSNP Id: rs1223138524
• MyVariant Identifiers: chr18:g.42800077G>T (hg19) ; chr18:g.45220112G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45220112G>T , CM000680.2:g.45220112G>T	GRCh38
NC_000018.9:g.42800077G>T , CM000680.1:g.42800077G>T	GRCh37
NC_000018.8:g.41054075G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586448.5:c.-125+6921G>T	ENSP00000465953.1:n.-125+6921G>T
NM_001242692.1:c.-125+6921G>T	NP_001229621.1:n.-125+6921G>T
XM_011526216.1:c.-251+6921G>T	XP_011524518.1:n.-251+6921G>T
XM_017026016.2:c.-125+6921G>T	XP_016881505.1:n.-125+6921G>T
XM_024451270.1:c.-125+6921G>T	XP_024307038.1:n.-125+6921G>T
XM_024451271.1:c.-125+6921G>T	XP_024307039.1:n.-125+6921G>T
NM_001242692.2:c.-125+6921G>T	NP_001229621.1:n.-125+6921G>T
NM_001371319.1:c.-125+6921G>T	NP_001358248.1:n.-125+6921G>T