Canonical Allele Identifier: CA2269091012
Gene: NACA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590813A= , CM000679.2:g.61590813A= GRCh38
NC_000017.10:g.59668174A= , CM000679.1:g.59668174A= GRCh37
NC_000017.9:g.57022956A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.368T= MANE Select ENSP00000427802.1:p.Phe123=
ENST00000521764.2:c.368T= ENSP00000427802.1:p.Phe123=
NM_199290.3:c.368T= NP_954984.1:p.Phe123=
NM_199290.4:c.368T= MANE Select NP_954984.1:p.Phe123=
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