Canonical Allele Identifier: CA557555669
Gene: SLC6A3 HGNC NCBI

Linked Data

gnomAD v2: 5-1443671-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1443556T>C , CM000667.2:g.1443556T>C GRCh38
NC_000005.9:g.1443671T>C , CM000667.1:g.1443671T>C GRCh37
NC_000005.8:g.1496671T>C NCBI36
NG_015885.1:g.6873A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.-45-314A>G MANE Select ENSP00000270349.9:n.-45-314A>G
ENST00000270349.11:c.-45-314A>G ENSP00000270349.9:n.-45-314A>G
NM_001044.4:c.-45-314A>G NP_001035.1:n.-45-314A>G
NM_001044.5:c.-45-314A>G MANE Select NP_001035.1:n.-45-314A>G