Canonical Allele Identifier: CA931959440
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Linked Data

dbSNP Id: rs1845271446

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102901649A>G , CM000672.2:g.102901649A>G GRCh38
NC_000010.10:g.104661406A>G , CM000672.1:g.104661406A>G GRCh37
NC_000010.9:g.104651396A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.*949A>G (AS3MT) MANE Select ENSP00000358896.3:n.*949A>G
ENST00000299353.6:c.*2084A>G (BORCS7-ASMT) ENSP00000299353.5:n.*2084A>G
ENST00000369880.7:c.*949A>G (AS3MT) ENSP00000358896.3:n.*949A>G
ENST00000615257.1:c.*384A>G (AS3MT) ENSP00000479361.1:n.*384A>G
NM_020682.3:c.*949A>G (AS3MT) NP_065733.2:n.*949A>G
NR_037644.1:n.2482A>G (BORCS7-ASMT)
XM_017017027.1:c.447-1139T>C XP_016872516.1:n.447-1139T>C
XR_001747577.1:n.169-1139T>C
XR_001747578.1:n.345-1139T>C
NM_020682.4:c.*949A>G (AS3MT) MANE Select NP_065733.2:n.*949A>G
NR_160733.1:n.169-1139T>C