Canonical Allele Identifier: CA421599787
Gene: ATP1A2 HGNC NCBI

Linked Data

gnomAD v4: 1-160127697-A-T
MyVariant Identifiers: chr1:g.160097487A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127697A>T , CM000663.2:g.160127697A>T GRCh38
NC_000001.10:g.160097487A>T , CM000663.1:g.160097487A>T GRCh37
NC_000001.9:g.158364111A>T NCBI36
NG_008014.1:g.16940A>T , LRG_6:g.16940A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.894A>T MANE Select ENSP00000354490.3:p.Val298=
ENST00000361216.7:c.894A>T ENSP00000354490.3:p.Val298=
ENST00000392233.7:c.894A>T ENSP00000376066.3:p.Val298=
ENST00000447527.1:c.26A>T
ENST00000472488.5:n.997A>T
NM_000702.3:c.894A>T NP_000693.1:p.Val298=
NM_000702.4:c.894A>T MANE Select NP_000693.1:p.Val298=
Search 100 bp 5'
Search 100 bp 3'