Canonical Allele Identifier: CA1932887268
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Linked Data

dbSNP Id: rs1845251667

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102900405T>C , CM000672.2:g.102900405T>C GRCh38
NC_000010.10:g.104660162T>C , CM000672.1:g.104660162T>C GRCh37
NC_000010.9:g.104650152T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.1021-188T>C (AS3MT) MANE Select ENSP00000358896.3:n.1021-188T>C
ENST00000299353.6:c.*1028-188T>C (BORCS7-ASMT) ENSP00000299353.5:n.*1028-188T>C
ENST00000369880.7:c.1021-188T>C (AS3MT) ENSP00000358896.3:n.1021-188T>C
ENST00000615257.1:c.*3-188T>C (AS3MT) ENSP00000479361.1:n.*3-188T>C
NM_020682.3:c.1021-188T>C (AS3MT) NP_065733.2:n.1021-188T>C
NR_037644.1:n.1426-188T>C (BORCS7-ASMT)
XM_017017027.1:c.*81A>G XP_016872516.1:n.*81A>G
XR_001747577.1:n.274A>G
XR_001747578.1:n.450A>G
NM_020682.4:c.1021-188T>C (AS3MT) MANE Select NP_065733.2:n.1021-188T>C
NR_160733.1:n.274A>G