Canonical Allele Identifier: CA1202196921

Gene: ATP1A2

Linked Data

• dbSNP Id: rs1652076400
• gnomAD v4: 1-160139823-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160139823A>G , CM000663.2:g.160139823A>G	GRCh38
NC_000001.10:g.160109613A>G , CM000663.1:g.160109613A>G	GRCh37
NC_000001.9:g.158376237A>G	NCBI36
NG_008014.1:g.29066A>G , LRG_6:g.29066A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361216.8:c.2943-70A>G MANE Select	ENSP00000354490.3:n.2943-70A>G
ENST00000361216.7:c.2943-70A>G	ENSP00000354490.3:n.2943-70A>G
ENST00000392233.7:c.2942+82A>G	ENSP00000376066.3:n.2942+82A>G
ENST00000447527.1:c.2024-70A>G
ENST00000463989.1:n.279-70A>G
NM_000702.3:c.2943-70A>G	NP_000693.1:n.2943-70A>G
NM_000702.4:c.2943-70A>G MANE Select	NP_000693.1:n.2943-70A>G