Canonical Allele Identifier: CA931959434
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Linked Data

dbSNP Id: rs1845271390

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102901638C>G , CM000672.2:g.102901638C>G GRCh38
NC_000010.10:g.104661395C>G , CM000672.1:g.104661395C>G GRCh37
NC_000010.9:g.104651385C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.*938C>G (AS3MT) MANE Select ENSP00000358896.3:n.*938C>G
ENST00000299353.6:c.*2073C>G (BORCS7-ASMT) ENSP00000299353.5:n.*2073C>G
ENST00000369880.7:c.*938C>G (AS3MT) ENSP00000358896.3:n.*938C>G
ENST00000615257.1:c.*373C>G (AS3MT) ENSP00000479361.1:n.*373C>G
NM_020682.3:c.*938C>G (AS3MT) NP_065733.2:n.*938C>G
NR_037644.1:n.2471C>G (BORCS7-ASMT)
XM_017017027.1:c.447-1128G>C XP_016872516.1:n.447-1128G>C
XR_001747577.1:n.169-1128G>C
XR_001747578.1:n.345-1128G>C
NM_020682.4:c.*938C>G (AS3MT) MANE Select NP_065733.2:n.*938C>G
NR_160733.1:n.169-1128G>C