Canonical Allele Identifier: CA743727582

Gene: SNTA1

Linked Data

• dbSNP Id: rs546697137
• gnomAD v3: 20-33439047-G-C
• gnomAD v4: 20-33439047-G-C
• MyVariant Identifiers: chr20:g.32026853G>C (hg19) ; chr20:g.33439047G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33439047G>C , CM000682.2:g.33439047G>C	GRCh38
NC_000020.10:g.32026853G>C , CM000682.1:g.32026853G>C	GRCh37
NC_000020.9:g.31490514G>C	NCBI36
NG_011622.1:g.9846C>G , LRG_332:g.9846C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.311-21C>G MANE Select	ENSP00000217381.2:n.311-21C>G
ENST00000217381.2:c.311-21C>G	ENSP00000217381.2:n.311-21C>G
NM_003098.2:c.311-21C>G , LRG_332t1:c.311-21C>G	NP_003089.1:n.311-21C>G
XM_005260517.1:c.311-21C>G	XP_005260574.1:n.311-21C>G
XM_011529007.1:c.311-21C>G	XP_011527309.1:n.311-21C>G
XM_011529008.1:c.311-21C>G	XP_011527310.1:n.311-21C>G
XR_936612.1:n.544-21C>G
XM_024451971.1:c.-17-21C>G	XP_024307739.1:n.-17-21C>G
NM_003098.3:c.311-21C>G MANE Select	NP_003089.1:n.311-21C>G