Canonical Allele Identifier: CA408634799
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33443596-G-T
MyVariant Identifiers: chr20:g.32031402G>T (hg19) chr20:g.33443596G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443596G>T , CM000682.2:g.33443596G>T GRCh38
NC_000020.10:g.32031402G>T , CM000682.1:g.32031402G>T GRCh37
NC_000020.9:g.31495063G>T NCBI36
NG_011622.1:g.5297C>A , LRG_332:g.5297C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.25C>A MANE Select ENSP00000217381.2:p.Arg9Ser
ENST00000217381.2:c.25C>A ENSP00000217381.2:p.Arg9Ser
NM_003098.2:c.25C>A , LRG_332t1:c.25C>A NP_003089.1:p.Arg9Ser
XM_005260517.1:c.25C>A XP_005260574.1:p.Arg9Ser
XM_011529007.1:c.25C>A XP_011527309.1:p.Arg9Ser
XM_011529008.1:c.25C>A XP_011527310.1:p.Arg9Ser
XR_936612.1:n.258C>A
NM_003098.3:c.25C>A MANE Select NP_003089.1:p.Arg9Ser
Search 100 bp 5'
Search 100 bp 3'