Canonical Allele Identifier: CA2577372553
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33412235-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33412235C>T , CM000682.2:g.33412235C>T GRCh38
NC_000020.10:g.32000041C>T , CM000682.1:g.32000041C>T GRCh37
NC_000020.9:g.31463702C>T NCBI36
NG_011622.1:g.36658G>A , LRG_332:g.36658G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.1040+61G>A MANE Select ENSP00000217381.2:n.1040+61G>A
ENST00000217381.2:c.1040+61G>A ENSP00000217381.2:n.1040+61G>A
NM_003098.2:c.1040+61G>A , LRG_332t1:c.1040+61G>A NP_003089.1:n.1040+61G>A
XM_005260517.1:c.1040+61G>A XP_005260574.1:n.1040+61G>A
XM_011529007.1:c.1040+61G>A XP_011527309.1:n.1040+61G>A
XM_011529008.1:c.1040+61G>A XP_011527310.1:n.1040+61G>A
XR_936612.1:n.1273+61G>A
XM_024451971.1:c.713+61G>A XP_024307739.1:n.713+61G>A
NM_003098.3:c.1040+61G>A MANE Select NP_003089.1:n.1040+61G>A
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