Canonical Allele Identifier: CA1335319125

Linked Data

dbSNP Id: rs1692123407

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232545863T>C , CM000664.2:g.232545863T>C GRCh38
NC_000002.11:g.233410573T>C , CM000664.1:g.233410573T>C GRCh37
NC_000002.10:g.233118817T>C NCBI36
NG_012954.1:g.11137T>C
NG_012954.2:g.11172T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000408957.7:c.*2244A>G (TIGD1) MANE Select ENSP00000386186.3:n.*2244A>G
ENST00000651502.1:c.*147T>C (CHRNG) MANE Select ENSP00000498757.1:n.*147T>C
ENST00000389494.7:c.*147T>C (CHRNG) ENSP00000374145.3:n.*147T>C
NM_005199.4:c.*147T>C (CHRNG) NP_005190.4:n.*147T>C
NM_005199.5:c.*147T>C (CHRNG) MANE Select NP_005190.4:n.*147T>C
NM_145702.4:c.*2244A>G (TIGD1) MANE Select NP_663748.1:n.*2244A>G