Canonical Allele Identifier: CA1308854481

Gene: CHN1

Linked Data

• dbSNP Id: rs1574028007

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799334T>C , CM000664.2:g.174799334T>C	GRCh38
NC_000002.11:g.175664062T>C , CM000664.1:g.175664062T>C	GRCh37
NC_000002.10:g.175372308T>C	NCBI36
NG_012642.1:g.211109A>G
NG_012642.2:g.211109A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295497.13:c.*782A>G	ENSP00000295497.7:n.*782A>G
ENST00000295497.12:c.*782A>G	ENSP00000295497.7:n.*782A>G
ENST00000409900.9:c.*782A>G MANE Select	ENSP00000386741.4:n.*782A>G
NM_001025201.3:c.*782A>G	NP_001020372.2:n.*782A>G
NM_001206602.1:c.*782A>G	NP_001193531.1:n.*782A>G
NM_001822.5:c.*782A>G	NP_001813.1:n.*782A>G
NR_038133.1:n.2028A>G
NM_001025201.4:c.*782A>G	NP_001020372.2:n.*782A>G
NM_001206602.2:c.*782A>G	NP_001193531.1:n.*782A>G
NM_001371513.1:c.*782A>G	NP_001358442.1:n.*782A>G
NM_001371514.1:c.*782A>G	NP_001358443.1:n.*782A>G
NM_001822.7:c.*782A>G MANE Select	NP_001813.1:n.*782A>G
NR_038133.2:n.2030A>G