Canonical Allele Identifier: CA510470078

Gene: SNTA1

Linked Data

• dbSNP Id: rs2146754311
• MyVariant Identifiers: chr20:g.31996549G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33408743G>C , CM000682.2:g.33408743G>C	GRCh38
NC_000020.10:g.31996549G>C , CM000682.1:g.31996549G>C	GRCh37
NC_000020.9:g.31460210G>C	NCBI36
NG_011622.1:g.40150C>G , LRG_332:g.40150C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000217381.3:c.1383C>G MANE Select	ENSP00000217381.2:p.Ala461=
ENST00000217381.2:c.1383C>G	ENSP00000217381.2:p.Ala461=
NM_003098.2:c.1383C>G , LRG_332t1:c.1383C>G	NP_003089.1:p.Ala461=
XM_005260517.1:c.1383C>G	XP_005260574.1:p.Ala461=
XM_011529007.1:c.1415C>G	XP_011527309.1:p.Pro472Arg
XM_011529008.1:c.1415C>G	XP_011527310.1:p.Pro472Arg
XR_936612.1:n.1419C>G
XM_024451971.1:c.1056C>G	XP_024307739.1:p.Ala352=
NM_003098.3:c.1383C>G MANE Select	NP_003089.1:p.Ala461=