Canonical Allele Identifier: CA2269091002
Gene: NACA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590793C= , CM000679.2:g.61590793C= GRCh38
NC_000017.10:g.59668154C= , CM000679.1:g.59668154C= GRCh37
NC_000017.9:g.57022936C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.388G= MANE Select ENSP00000427802.1:p.Asp130=
ENST00000521764.2:c.388G= ENSP00000427802.1:p.Asp130=
NM_199290.3:c.388G= NP_954984.1:p.Asp130=
NM_199290.4:c.388G= MANE Select NP_954984.1:p.Asp130=
Search 100 bp 5'
Search 100 bp 3'