Canonical Allele Identifier: CA2269091032
Gene: NACA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590850C= , CM000679.2:g.61590850C= GRCh38
NC_000017.10:g.59668211C= , CM000679.1:g.59668211C= GRCh37
NC_000017.9:g.57022993C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.331G= MANE Select ENSP00000427802.1:p.Val111=
ENST00000521764.2:c.331G= ENSP00000427802.1:p.Val111=
NM_199290.3:c.331G= NP_954984.1:p.Val111=
NM_199290.4:c.331G= MANE Select NP_954984.1:p.Val111=
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