Canonical Allele Identifier: CA1939106021
Gene: SLC18A2 HGNC NCBI

Linked Data

dbSNP Id: rs2090996559
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117263154T>C , CM000672.2:g.117263154T>C GRCh38
NC_000010.10:g.119022665T>C , CM000672.1:g.119022665T>C GRCh37
NC_000010.9:g.119012655T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.992-3579T>C MANE Select ENSP00000496339.1:n.992-3579T>C
ENST00000298472.9:c.992-3579T>C ENSP00000298472.5:n.992-3579T>C
ENST00000497497.1:n.1408-3579T>C
NM_003054.4:c.992-3579T>C NP_003045.2:n.992-3579T>C
NM_003054.5:c.992-3579T>C NP_003045.2:n.992-3579T>C
NM_003054.6:c.992-3579T>C MANE Select NP_003045.2:n.992-3579T>C
Search 100 bp 5'
Search 100 bp 3'