Canonical Allele Identifier: CA371446834
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87656043A>T (hg19) chr8:g.86643815A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86643815A>T , CM000670.2:g.86643815A>T GRCh38
NC_000008.10:g.87656043A>T , CM000670.1:g.87656043A>T GRCh37
NC_000008.9:g.87725159A>T NCBI36
NG_016980.1:g.104861T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1114T>A MANE Select ENSP00000316605.5:p.Tyr372Asn
ENST00000681546.1:n.934T>A
ENST00000681746.1:c.1114T>A ENSP00000505959.1:p.Tyr372Asn
ENST00000320005.5:c.1114T>A ENSP00000316605.5:p.Tyr372Asn
NM_019098.4:c.1114T>A NP_061971.3:p.Tyr372Asn
XM_011517138.1:c.700T>A XP_011515440.1:p.Tyr234Asn
XM_011517138.2:c.700T>A XP_011515440.1:p.Tyr234Asn
NM_019098.5:c.1114T>A MANE Select NP_061971.3:p.Tyr372Asn
Search 100 bp 5'
Search 100 bp 3'