Canonical Allele Identifier: CA379664752
Gene: CTR9 HGNC NCBI

Linked Data

dbSNP Id: rs1863014355

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763739A>G , CM000673.2:g.10763739A>G GRCh38
NC_000011.9:g.10785286A>G , CM000673.1:g.10785286A>G GRCh37
NC_000011.8:g.10741862A>G NCBI36
NG_051671.1:g.17753A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1054A>G MANE Select ENSP00000355013.2:p.Ile352Val
ENST00000361367.6:c.1054A>G ENSP00000355013.2:p.Ile352Val
NM_014633.4:c.1054A>G NP_055448.1:p.Ile352Val
NM_001346279.1:c.1054A>G NP_001333208.1:p.Ile352Val
NM_014633.5:c.1054A>G MANE Select NP_055448.1:p.Ile352Val
NM_001346279.2:c.1054A>G NP_001333208.1:p.Ile352Val