Canonical Allele Identifier: CA2673095513
Gene: SLC6A3 HGNC NCBI

Linked Data

gnomAD v4: 5-1414551-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414551T>G , CM000667.2:g.1414551T>G GRCh38
NC_000005.9:g.1414666T>G , CM000667.1:g.1414666T>G GRCh37
NC_000005.8:g.1467666T>G NCBI36
NG_015885.1:g.35878A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1156+140A>C MANE Select ENSP00000270349.9:n.1156+140A>C
ENST00000270349.11:c.1156+140A>C ENSP00000270349.9:n.1156+140A>C
NM_001044.4:c.1156+140A>C NP_001035.1:n.1156+140A>C
NM_001044.5:c.1156+140A>C MANE Select NP_001035.1:n.1156+140A>C