Canonical Allele Identifier: CA5885017
Gene: CTR9 HGNC NCBI

Linked Data

dbSNP Id: rs767354168
ExAC: 11:10785318 G / A
gnomAD v2: 11-10785318-G-A
gnomAD v4: 11-10763771-G-A
MyVariant Identifiers: chr11:g.10785318G>A (hg19) chr11:g.10763771G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763771G>A , CM000673.2:g.10763771G>A GRCh38
NC_000011.9:g.10785318G>A , CM000673.1:g.10785318G>A GRCh37
NC_000011.8:g.10741894G>A NCBI36
NG_051671.1:g.17785G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1086G>A MANE Select ENSP00000355013.2:p.Gln362=
ENST00000361367.6:c.1086G>A ENSP00000355013.2:p.Gln362=
NM_014633.4:c.1086G>A NP_055448.1:p.Gln362=
NM_001346279.1:c.1086G>A NP_001333208.1:p.Gln362=
NM_014633.5:c.1086G>A MANE Select NP_055448.1:p.Gln362=
NM_001346279.2:c.1086G>A NP_001333208.1:p.Gln362=
Search 100 bp 5'
Search 100 bp 3'