Canonical Allele Identifier: CA180366901
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs970343698
MyVariant Identifiers: chr8:g.87683542G>T (hg19) chr8:g.86671314G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671314G>T , CM000670.2:g.86671314G>T GRCh38
NC_000008.10:g.87683542G>T , CM000670.1:g.87683542G>T GRCh37
NC_000008.9:g.87752658G>T NCBI36
NG_016980.1:g.77362C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.339-216C>A MANE Select ENSP00000316605.5:n.339-216C>A
ENST00000680314.1:n.100-216C>A
ENST00000681746.1:c.339-216C>A ENSP00000505959.1:n.339-216C>A
ENST00000320005.5:c.339-216C>A ENSP00000316605.5:n.339-216C>A
NM_019098.4:c.339-216C>A NP_061971.3:n.339-216C>A
XM_011517138.1:c.-76-216C>A XP_011515440.1:n.-76-216C>A
XM_011517138.2:c.-76-216C>A XP_011515440.1:n.-76-216C>A
NM_019098.5:c.339-216C>A MANE Select NP_061971.3:n.339-216C>A
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