Canonical Allele Identifier: CA13360095

Gene: SLC18A2

Linked Data

• dbSNP Id: rs363276
• gnomAD v2: 10-119033809-T-C
• gnomAD v3: 10-117274298-T-C
• gnomAD v4: 10-117274298-T-C
• MyVariant Identifiers: chr10:g.119033809T>C (hg19) ; chr10:g.117274298T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117274298T>C , CM000672.2:g.117274298T>C	GRCh38
NC_000010.10:g.119033809T>C , CM000672.1:g.119033809T>C	GRCh37
NC_000010.9:g.119023799T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000644641.2:c.1441-2864T>C MANE Select	ENSP00000496339.1:n.1441-2864T>C
ENST00000298472.9:c.1441-2864T>C	ENSP00000298472.5:n.1441-2864T>C
ENST00000497497.1:n.1857-2864T>C
NM_003054.4:c.1441-2864T>C	NP_003045.2:n.1441-2864T>C
NM_003054.5:c.1441-2864T>C	NP_003045.2:n.1441-2864T>C
NM_003054.6:c.1441-2864T>C MANE Select	NP_003045.2:n.1441-2864T>C