Canonical Allele Identifier: CA985260645
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs879056164
gnomAD v3: 17-61590528-G-C
gnomAD v4: 17-61590528-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590528G>C , CM000679.2:g.61590528G>C GRCh38
NC_000017.10:g.59667889G>C , CM000679.1:g.59667889G>C GRCh37
NC_000017.9:g.57022671G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.*5C>G MANE Select ENSP00000427802.1:n.*5C>G
ENST00000521764.2:c.*5C>G ENSP00000427802.1:n.*5C>G
NM_199290.3:c.*5C>G NP_954984.1:n.*5C>G
NM_199290.4:c.*5C>G MANE Select NP_954984.1:n.*5C>G
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