Canonical Allele Identifier: CA5496743
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 2967752
ClinVar RCV Id: RCV003826414
dbSNP Id: rs768880483
ExAC: 10:50819104 A / G
gnomAD v2: 10-50819104-A-G
gnomAD v3: 10-49611058-A-G
gnomAD v4: 10-49611058-A-G
MyVariant Identifiers: chr10:g.50819104A>G (hg19) chr10:g.49611058A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49611058A>G , CM000672.2:g.49611058A>G GRCh38
NC_000010.10:g.50819104A>G , CM000672.1:g.50819104A>G GRCh37
NC_000010.9:g.50489110A>G NCBI36
NG_011797.1:g.6964A>G
NG_053144.1:g.5758A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374115.5:c.318A>G (SLC18A3) MANE Select ENSP00000363229.3:p.Pro106=
ENST00000339797.5:c.-69+1859A>G (CHAT) ENSP00000343486.1:n.-69+1859A>G
ENST00000374115.4:c.318A>G (SLC18A3) ENSP00000363229.3:p.Pro106=
NM_003055.2:c.318A>G (SLC18A3) NP_003046.2:p.Pro106=
NM_020984.3:c.-69+1859A>G (CHAT) NP_066264.3:n.-69+1859A>G
NM_003055.3:c.318A>G (SLC18A3) MANE Select NP_003046.2:p.Pro106=
NM_020984.4:c.-69+1859A>G (CHAT) NP_066264.4:n.-69+1859A>G
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