Canonical Allele Identifier: CA400784158
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59668175A>G (hg19) chr17:g.61590814A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590814A>G , CM000679.2:g.61590814A>G GRCh38
NC_000017.10:g.59668175A>G , CM000679.1:g.59668175A>G GRCh37
NC_000017.9:g.57022957A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.367T>C MANE Select ENSP00000427802.1:p.Phe123Leu
ENST00000521764.2:c.367T>C ENSP00000427802.1:p.Phe123Leu
NM_199290.3:c.367T>C NP_954984.1:p.Phe123Leu
NM_199290.4:c.367T>C MANE Select NP_954984.1:p.Phe123Leu
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