Canonical Allele Identifier: CA2573931563
Gene: ATP1A2 HGNC NCBI

Linked Data

gnomAD v4: 1-160140011-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160140011A>G , CM000663.2:g.160140011A>G GRCh38
NC_000001.10:g.160109801A>G , CM000663.1:g.160109801A>G GRCh37
NC_000001.9:g.158376425A>G NCBI36
NG_008014.1:g.29254A>G , LRG_6:g.29254A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.3034+27A>G MANE Select ENSP00000354490.3:n.3034+27A>G
ENST00000361216.7:c.3034+27A>G ENSP00000354490.3:n.3034+27A>G
ENST00000392233.7:c.3001+27A>G ENSP00000376066.3:n.3001+27A>G
ENST00000447527.1:c.2115+27A>G
ENST00000459972.1:n.26+27A>G
ENST00000463989.1:n.397A>G
NM_000702.3:c.3034+27A>G NP_000693.1:n.3034+27A>G
NM_000702.4:c.3034+27A>G MANE Select NP_000693.1:n.3034+27A>G
Search 100 bp 5'
Search 100 bp 3'