Canonical Allele Identifier: CA804559261
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1349847740

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1394210A>G , CM000667.2:g.1394210A>G GRCh38
NC_000005.9:g.1394325A>G , CM000667.1:g.1394325A>G GRCh37
NC_000005.8:g.1447325A>G NCBI36
NG_015885.1:g.56219T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.*525T>C MANE Select ENSP00000270349.9:n.*525T>C
ENST00000270349.11:c.*525T>C ENSP00000270349.9:n.*525T>C
ENST00000512002.2:n.769T>C
NM_001044.4:c.*525T>C NP_001035.1:n.*525T>C
NM_001044.5:c.*525T>C MANE Select NP_001035.1:n.*525T>C