Canonical Allele Identifier: CA371448294
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86647875-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647875A>G , CM000670.2:g.86647875A>G GRCh38
NC_000008.10:g.87660103A>G , CM000670.1:g.87660103A>G GRCh37
NC_000008.9:g.87729219A>G NCBI36
NG_016980.1:g.100801T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.916T>C MANE Select ENSP00000316605.5:p.Ser306Pro
ENST00000681546.1:n.736T>C
ENST00000681746.1:c.916T>C ENSP00000505959.1:p.Ser306Pro
ENST00000320005.5:c.916T>C ENSP00000316605.5:p.Ser306Pro
NM_019098.4:c.916T>C NP_061971.3:p.Ser306Pro
XM_011517138.1:c.502T>C XP_011515440.1:p.Ser168Pro
XM_011517138.2:c.502T>C XP_011515440.1:p.Ser168Pro
NM_019098.5:c.916T>C MANE Select NP_061971.3:p.Ser306Pro