Canonical Allele Identifier: CA374047532
Gene: NINJ1 HGNC NCBI

Linked Data

dbSNP Id: rs2275848
gnomAD v4: 9-93125038-G-C
MyVariant Identifiers: chr9:g.95887320G>C (hg19) chr9:g.93125038G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93125038G>C , CM000671.2:g.93125038G>C GRCh38
NC_000009.11:g.95887320G>C , CM000671.1:g.95887320G>C GRCh37
NC_000009.10:g.94927141G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375446.5:c.329C>G MANE Select ENSP00000364595.4:p.Ala110Gly
ENST00000375446.4:c.329C>G ENSP00000364595.4:p.Ala110Gly
ENST00000461162.5:n.388C>G
ENST00000470314.5:n.297C>G
ENST00000489274.1:n.1153C>G
NM_004148.3:c.329C>G NP_004139.2:p.Ala110Gly
XM_011518716.1:c.179C>G XP_011517018.1:p.Ala60Gly
NM_004148.4:c.329C>G MANE Select NP_004139.2:p.Ala110Gly
Search 100 bp 5'
Search 100 bp 3'