Canonical Allele Identifier: CA2652477476
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33412236-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33412236C>T , CM000682.2:g.33412236C>T GRCh38
NC_000020.10:g.32000042C>T , CM000682.1:g.32000042C>T GRCh37
NC_000020.9:g.31463703C>T NCBI36
NG_011622.1:g.36657G>A , LRG_332:g.36657G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.1040+60G>A MANE Select ENSP00000217381.2:n.1040+60G>A
ENST00000217381.2:c.1040+60G>A ENSP00000217381.2:n.1040+60G>A
NM_003098.2:c.1040+60G>A , LRG_332t1:c.1040+60G>A NP_003089.1:n.1040+60G>A
XM_005260517.1:c.1040+60G>A XP_005260574.1:n.1040+60G>A
XM_011529007.1:c.1040+60G>A XP_011527309.1:n.1040+60G>A
XM_011529008.1:c.1040+60G>A XP_011527310.1:n.1040+60G>A
XR_936612.1:n.1273+60G>A
XM_024451971.1:c.713+60G>A XP_024307739.1:n.713+60G>A
NM_003098.3:c.1040+60G>A MANE Select NP_003089.1:n.1040+60G>A
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