Canonical Allele Identifier: CA931959445
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Linked Data

dbSNP Id: rs1845271706

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102901662G>A , CM000672.2:g.102901662G>A GRCh38
NC_000010.10:g.104661419G>A , CM000672.1:g.104661419G>A GRCh37
NC_000010.9:g.104651409G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.*962G>A (AS3MT) MANE Select ENSP00000358896.3:n.*962G>A
ENST00000299353.6:c.*2097G>A (BORCS7-ASMT) ENSP00000299353.5:n.*2097G>A
ENST00000369880.7:c.*962G>A (AS3MT) ENSP00000358896.3:n.*962G>A
ENST00000615257.1:c.*397G>A (AS3MT) ENSP00000479361.1:n.*397G>A
NM_020682.3:c.*962G>A (AS3MT) NP_065733.2:n.*962G>A
NR_037644.1:n.2495G>A (BORCS7-ASMT)
XM_017017027.1:c.447-1152C>T XP_016872516.1:n.447-1152C>T
XR_001747577.1:n.169-1152C>T
XR_001747578.1:n.345-1152C>T
NM_020682.4:c.*962G>A (AS3MT) MANE Select NP_065733.2:n.*962G>A
NR_160733.1:n.169-1152C>T