Canonical Allele Identifier: CA1335319123

Linked Data

dbSNP Id: rs1692123365

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232545859A>T , CM000664.2:g.232545859A>T GRCh38
NC_000002.11:g.233410569A>T , CM000664.1:g.233410569A>T GRCh37
NC_000002.10:g.233118813A>T NCBI36
NG_012954.1:g.11133A>T
NG_012954.2:g.11168A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000408957.7:c.*2248T>A (TIGD1) MANE Select ENSP00000386186.3:n.*2248T>A
ENST00000651502.1:c.*143A>T (CHRNG) MANE Select ENSP00000498757.1:n.*143A>T
ENST00000389494.7:c.*143A>T (CHRNG) ENSP00000374145.3:n.*143A>T
NM_005199.4:c.*143A>T (CHRNG) NP_005190.4:n.*143A>T
NM_005199.5:c.*143A>T (CHRNG) MANE Select NP_005190.4:n.*143A>T
NM_145702.4:c.*2248T>A (TIGD1) MANE Select NP_663748.1:n.*2248T>A