Canonical Allele Identifier: CA376715931

Gene: SLC18A3 CHAT

Linked Data

• dbSNP Id: rs1190038791
• gnomAD v2: 10-50818911-C-T
• gnomAD v4: 10-49610865-C-T
• MyVariant Identifiers: chr10:g.50818911C>T (hg19) ; chr10:g.49610865C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49610865C>T , CM000672.2:g.49610865C>T	GRCh38
NC_000010.10:g.50818911C>T , CM000672.1:g.50818911C>T	GRCh37
NC_000010.9:g.50488917C>T	NCBI36
NG_011797.1:g.6771C>T
NG_053144.1:g.5565C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374115.5:c.125C>T (SLC18A3) MANE Select	ENSP00000363229.3:p.Ala42Val
ENST00000339797.5:c.-69+1666C>T (CHAT)	ENSP00000343486.1:n.-69+1666C>T
ENST00000374115.4:c.125C>T (SLC18A3)	ENSP00000363229.3:p.Ala42Val
NM_003055.2:c.125C>T (SLC18A3)	NP_003046.2:p.Ala42Val
NM_020984.3:c.-69+1666C>T (CHAT)	NP_066264.3:n.-69+1666C>T
NM_003055.3:c.125C>T (SLC18A3) MANE Select	NP_003046.2:p.Ala42Val
NM_020984.4:c.-69+1666C>T (CHAT)	NP_066264.4:n.-69+1666C>T