Canonical Allele Identifier: CA1017044181
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1018674417
gnomAD v3: 20-33443712-G-C
gnomAD v4: 20-33443712-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443712G>C , CM000682.2:g.33443712G>C GRCh38
NC_000020.10:g.32031518G>C , CM000682.1:g.32031518G>C GRCh37
NC_000020.9:g.31495179G>C NCBI36
NG_011622.1:g.5181C>G , LRG_332:g.5181C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.-92C>G MANE Select ENSP00000217381.2:n.-92C>G
ENST00000217381.2:c.-92C>G ENSP00000217381.2:n.-92C>G
NM_003098.2:c.-92C>G , LRG_332t1:c.-92C>G NP_003089.1:n.-92C>G
XM_005260517.1:c.-92C>G XP_005260574.1:n.-92C>G
XM_011529007.1:c.-92C>G XP_011527309.1:n.-92C>G
XM_011529008.1:c.-92C>G XP_011527310.1:n.-92C>G
XR_936612.1:n.142C>G
NM_003098.3:c.-92C>G MANE Select NP_003089.1:n.-92C>G
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