Canonical Allele Identifier: CA343243837
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160100083T>C (hg19) chr1:g.160130293T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130293T>C , CM000663.2:g.160130293T>C GRCh38
NC_000001.10:g.160100083T>C , CM000663.1:g.160100083T>C GRCh37
NC_000001.9:g.158366707T>C NCBI36
NG_008014.1:g.19536T>C , LRG_6:g.19536T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.1651+2T>C MANE Select ENSP00000354490.3:n.1651+2T>C
ENST00000361216.7:c.1651+2T>C ENSP00000354490.3:n.1651+2T>C
ENST00000392233.7:c.1651+2T>C ENSP00000376066.3:n.1651+2T>C
ENST00000447527.1:c.783+2T>C
ENST00000472488.5:n.1754+2T>C
NM_000702.3:c.1651+2T>C NP_000693.1:n.1651+2T>C
NM_000702.4:c.1651+2T>C MANE Select NP_000693.1:n.1651+2T>C
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