Canonical Allele Identifier: CA2269090877
Gene: NACA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590550T= , CM000679.2:g.61590550T= GRCh38
NC_000017.10:g.59667911T= , CM000679.1:g.59667911T= GRCh37
NC_000017.9:g.57022693T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.631A= MANE Select ENSP00000427802.1:p.Met211=
ENST00000521764.2:c.631A= ENSP00000427802.1:p.Met211=
NM_199290.3:c.631A= NP_954984.1:p.Met211=
NM_199290.4:c.631A= MANE Select NP_954984.1:p.Met211=
Search 100 bp 5'
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