Canonical Allele Identifier: CA15412766

Gene: FYB1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.39105492C>T , CM000667.2:g.39105492C>T	GRCh38
NC_000005.9:g.39105594C>T , CM000667.1:g.39105594C>T	GRCh37
NC_000005.8:g.39141351C>T	NCBI36
NG_029596.1:g.170166G>A
NG_029596.2:g.170166G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351578.12:c.*1951G>A	ENSP00000316460.7:n.*1951G>A
ENST00000512982.4:c.*1951G>A MANE Select	ENSP00000425845.3:n.*1951G>A
ENST00000646045.2:c.*1951G>A	ENSP00000493623.1:n.*1951G>A
ENST00000351578.10:c.*1951G>A	ENSP00000316460.7:n.*1951G>A
NM_001243093.1:c.*1951G>A	NP_001230022.1:n.*1951G>A
NM_001465.4:c.*1951G>A	NP_001456.3:n.*1951G>A
NM_199335.3:c.*1951G>A	NP_955367.1:n.*1951G>A
XM_006714464.2:c.*1951G>A	XP_006714527.1:n.*1951G>A
XM_006714465.2:c.*1951G>A	XP_006714528.1:n.*1951G>A
XM_006714466.2:c.*1951G>A	XP_006714529.1:n.*1951G>A
XM_011514008.1:c.*1951G>A	XP_011512310.1:n.*1951G>A
XM_011514009.1:c.*1951G>A	XP_011512311.1:n.*1951G>A
XM_011514010.1:c.*1951G>A	XP_011512312.1:n.*1951G>A
XM_011514011.1:c.*1951G>A	XP_011512313.1:n.*1951G>A
NM_001349333.1:c.*1951G>A	NP_001336262.1:n.*1951G>A
NM_001465.5:c.*1951G>A	NP_001456.3:n.*1951G>A
NM_018594.2:c.*1951G>A	NP_061064.2:n.*1951G>A
NM_199335.4:c.*1951G>A	NP_955367.1:n.*1951G>A
XM_006714464.3:c.*1951G>A	XP_006714527.1:n.*1951G>A
XM_011514008.3:c.*1951G>A	XP_011512310.1:n.*1951G>A
XM_011514011.2:c.*1951G>A	XP_011512313.1:n.*1951G>A
NM_001243093.2:c.*1951G>A	NP_001230022.1:n.*1951G>A
NM_001349333.2:c.*1951G>A	NP_001336262.1:n.*1951G>A
NM_001465.6:c.*1951G>A MANE Select	NP_001456.3:n.*1951G>A
NM_199335.5:c.*1951G>A	NP_955367.1:n.*1951G>A