Canonical Allele Identifier: CA400784114
Gene: NACA2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.388G>T MANE Select ENSP00000427802.1:p.Asp130Tyr
ENST00000521764.2:c.388G>T ENSP00000427802.1:p.Asp130Tyr
NM_199290.3:c.388G>T NP_954984.1:p.Asp130Tyr
NM_199290.4:c.388G>T MANE Select NP_954984.1:p.Asp130Tyr