Canonical Allele Identifier: CA371450224
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87683265T>C (hg19) chr8:g.86671037T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671037T>C , CM000670.2:g.86671037T>C GRCh38
NC_000008.10:g.87683265T>C , CM000670.1:g.87683265T>C GRCh37
NC_000008.9:g.87752381T>C NCBI36
NG_016980.1:g.77639A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.400A>G MANE Select ENSP00000316605.5:p.Asn134Asp
ENST00000680314.1:n.161A>G
ENST00000681746.1:c.400A>G ENSP00000505959.1:p.Asn134Asp
ENST00000320005.5:c.400A>G ENSP00000316605.5:p.Asn134Asp
NM_019098.4:c.400A>G NP_061971.3:p.Asn134Asp
XM_011517138.1:c.-15A>G XP_011515440.1:n.-15A>G
XM_011517138.2:c.-15A>G XP_011515440.1:n.-15A>G
NM_019098.5:c.400A>G MANE Select NP_061971.3:p.Asn134Asp
Search 100 bp 5'
Search 100 bp 3'