Canonical Allele Identifier: CA1202196786

Gene: ATP1A2

Linked Data

• dbSNP Id: rs1652063831

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160139498A>G , CM000663.2:g.160139498A>G	GRCh38
NC_000001.10:g.160109288A>G , CM000663.1:g.160109288A>G	GRCh37
NC_000001.9:g.158375912A>G	NCBI36
NG_008014.1:g.28741A>G , LRG_6:g.28741A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.2841-142A>G MANE Select	ENSP00000354490.3:n.2841-142A>G
ENST00000361216.7:c.2841-142A>G	ENSP00000354490.3:n.2841-142A>G
ENST00000392233.7:c.2841-142A>G	ENSP00000376066.3:n.2841-142A>G
ENST00000447527.1:c.1922-142A>G
ENST00000463989.1:n.177-142A>G
NM_000702.3:c.2841-142A>G	NP_000693.1:n.2841-142A>G
NM_000702.4:c.2841-142A>G MANE Select	NP_000693.1:n.2841-142A>G