Canonical Allele Identifier: CA2652478032
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33438814-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438814T>C , CM000682.2:g.33438814T>C GRCh38
NC_000020.10:g.32026620T>C , CM000682.1:g.32026620T>C GRCh37
NC_000020.9:g.31490281T>C NCBI36
NG_011622.1:g.10079A>G , LRG_332:g.10079A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.496+27A>G MANE Select ENSP00000217381.2:n.496+27A>G
ENST00000217381.2:c.496+27A>G ENSP00000217381.2:n.496+27A>G
NM_003098.2:c.496+27A>G , LRG_332t1:c.496+27A>G NP_003089.1:n.496+27A>G
XM_005260517.1:c.496+27A>G XP_005260574.1:n.496+27A>G
XM_011529007.1:c.496+27A>G XP_011527309.1:n.496+27A>G
XM_011529008.1:c.496+27A>G XP_011527310.1:n.496+27A>G
XR_936612.1:n.729+27A>G
XM_024451971.1:c.169+27A>G XP_024307739.1:n.169+27A>G
NM_003098.3:c.496+27A>G MANE Select NP_003089.1:n.496+27A>G
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