Canonical Allele Identifier: CA1558462340
Gene: DHFR HGNC NCBI

Linked Data

dbSNP Id: rs1580508453

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628880A>G , CM000667.2:g.80628880A>G GRCh38
NC_000005.9:g.79924699A>G , CM000667.1:g.79924699A>G GRCh37
NC_000005.8:g.79960455A>G NCBI36
NG_023304.1:g.31102T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.*207T>C MANE Select ENSP00000396308.2:n.*207T>C
ENST00000439211.6:c.*207T>C ENSP00000396308.2:n.*207T>C
ENST00000504396.1:c.*207T>C ENSP00000421334.1:n.*207T>C
ENST00000505337.5:c.*107T>C ENSP00000426474.1:n.*107T>C
ENST00000511032.5:c.*265T>C ENSP00000422732.1:n.*265T>C
ENST00000513048.5:n.652T>C
NM_000791.3:c.*207T>C NP_000782.1:n.*207T>C
NM_001290354.1:c.*207T>C NP_001277283.1:n.*207T>C
NM_001290357.1:c.*265T>C NP_001277286.1:n.*265T>C
NR_110936.1:n.1086T>C
NM_000791.4:c.*207T>C MANE Select NP_000782.1:n.*207T>C
NM_001290354.2:c.*207T>C NP_001277283.1:n.*207T>C
NM_001290357.2:c.*265T>C NP_001277286.1:n.*265T>C
NR_110936.2:n.1088T>C