Canonical Allele Identifier: CA1202196922
Gene: ATP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160139826G= , CM000663.2:g.160139826G= GRCh38
NC_000001.10:g.160109616G= , CM000663.1:g.160109616G= GRCh37
NC_000001.9:g.158376240G= NCBI36
NG_008014.1:g.29069G= , LRG_6:g.29069G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.2943-67G= MANE Select ENSP00000354490.3:n.2943-67G=
ENST00000361216.7:c.2943-67G= ENSP00000354490.3:n.2943-67G=
ENST00000392233.7:c.2942+85G= ENSP00000376066.3:n.2942+85G=
ENST00000447527.1:c.2024-67G=
ENST00000463989.1:n.279-67G=
NM_000702.3:c.2943-67G= NP_000693.1:n.2943-67G=
NM_000702.4:c.2943-67G= MANE Select NP_000693.1:n.2943-67G=
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