Canonical Allele Identifier: CA2652477456
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33412224-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33412224A>G , CM000682.2:g.33412224A>G GRCh38
NC_000020.10:g.32000030A>G , CM000682.1:g.32000030A>G GRCh37
NC_000020.9:g.31463691A>G NCBI36
NG_011622.1:g.36669T>C , LRG_332:g.36669T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.1040+72T>C MANE Select ENSP00000217381.2:n.1040+72T>C
ENST00000217381.2:c.1040+72T>C ENSP00000217381.2:n.1040+72T>C
NM_003098.2:c.1040+72T>C , LRG_332t1:c.1040+72T>C NP_003089.1:n.1040+72T>C
XM_005260517.1:c.1040+72T>C XP_005260574.1:n.1040+72T>C
XM_011529007.1:c.1040+72T>C XP_011527309.1:n.1040+72T>C
XM_011529008.1:c.1040+72T>C XP_011527310.1:n.1040+72T>C
XR_936612.1:n.1273+72T>C
XM_024451971.1:c.713+72T>C XP_024307739.1:n.713+72T>C
NM_003098.3:c.1040+72T>C MANE Select NP_003089.1:n.1040+72T>C
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