Canonical Allele Identifier: CA408634529

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33443521-T-C
• MyVariant Identifiers: chr20:g.32031327T>C (hg19) ; chr20:g.33443521T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443521T>C , CM000682.2:g.33443521T>C	GRCh38
NC_000020.10:g.32031327T>C , CM000682.1:g.32031327T>C	GRCh37
NC_000020.9:g.31494988T>C	NCBI36
NG_011622.1:g.5372A>G , LRG_332:g.5372A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.100A>G MANE Select	ENSP00000217381.2:p.Ser34Gly
ENST00000217381.2:c.100A>G	ENSP00000217381.2:p.Ser34Gly
NM_003098.2:c.100A>G , LRG_332t1:c.100A>G	NP_003089.1:p.Ser34Gly
XM_005260517.1:c.100A>G	XP_005260574.1:p.Ser34Gly
XM_011529007.1:c.100A>G	XP_011527309.1:p.Ser34Gly
XM_011529008.1:c.100A>G	XP_011527310.1:p.Ser34Gly
XR_936612.1:n.333A>G
NM_003098.3:c.100A>G MANE Select	NP_003089.1:p.Ser34Gly