Canonical Allele Identifier: CA408633686
Gene: SNTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.32026833C>G (hg19) chr20:g.33439027C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33439027C>G , CM000682.2:g.33439027C>G GRCh38
NC_000020.10:g.32026833C>G , CM000682.1:g.32026833C>G GRCh37
NC_000020.9:g.31490494C>G NCBI36
NG_011622.1:g.9866G>C , LRG_332:g.9866G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.311-1G>C MANE Select ENSP00000217381.2:n.311-1G>C
ENST00000217381.2:c.311-1G>C ENSP00000217381.2:n.311-1G>C
NM_003098.2:c.311-1G>C , LRG_332t1:c.311-1G>C NP_003089.1:n.311-1G>C
XM_005260517.1:c.311-1G>C XP_005260574.1:n.311-1G>C
XM_011529007.1:c.311-1G>C XP_011527309.1:n.311-1G>C
XM_011529008.1:c.311-1G>C XP_011527310.1:n.311-1G>C
XR_936612.1:n.544-1G>C
XM_024451971.1:c.-17-1G>C XP_024307739.1:n.-17-1G>C
NM_003098.3:c.311-1G>C MANE Select NP_003089.1:n.311-1G>C
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