Canonical Allele Identifier: CA2207124539
Gene: EMP2 HGNC NCBI

Linked Data

dbSNP Id: rs1052719950
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10539315G>T , CM000678.2:g.10539315G>T GRCh38
NC_000016.9:g.10633172G>T , CM000678.1:g.10633172G>T GRCh37
NC_000016.8:g.10540673G>T NCBI36
NG_042058.1:g.46402C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359543.8:c.170-1241C>A MANE Select ENSP00000352540.3:n.170-1241C>A
ENST00000359543.7:c.170-1241C>A ENSP00000352540.3:n.170-1241C>A
ENST00000536829.1:c.170-1241C>A ENSP00000445712.1:n.170-1241C>A
NM_001424.4:c.170-1241C>A NP_001415.1:n.170-1241C>A
NM_001424.5:c.170-1241C>A NP_001415.1:n.170-1241C>A
XM_006720864.2:c.170-1241C>A XP_006720927.1:n.170-1241C>A
XM_006720864.3:c.170-1241C>A XP_006720927.1:n.170-1241C>A
NM_001424.6:c.170-1241C>A MANE Select NP_001415.1:n.170-1241C>A
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