Canonical Allele Identifier: CA1558462348
Gene: DHFR HGNC NCBI

Linked Data

dbSNP Id: rs1747952151

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628884A>T , CM000667.2:g.80628884A>T GRCh38
NC_000005.9:g.79924703A>T , CM000667.1:g.79924703A>T GRCh37
NC_000005.8:g.79960459A>T NCBI36
NG_023304.1:g.31098T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.*203T>A MANE Select ENSP00000396308.2:n.*203T>A
ENST00000439211.6:c.*203T>A ENSP00000396308.2:n.*203T>A
ENST00000504396.1:c.*203T>A ENSP00000421334.1:n.*203T>A
ENST00000505337.5:c.*103T>A ENSP00000426474.1:n.*103T>A
ENST00000511032.5:c.*261T>A ENSP00000422732.1:n.*261T>A
ENST00000513048.5:n.648T>A
NM_000791.3:c.*203T>A NP_000782.1:n.*203T>A
NM_001290354.1:c.*203T>A NP_001277283.1:n.*203T>A
NM_001290357.1:c.*261T>A NP_001277286.1:n.*261T>A
NR_110936.1:n.1082T>A
NM_000791.4:c.*203T>A MANE Select NP_000782.1:n.*203T>A
NM_001290354.2:c.*203T>A NP_001277283.1:n.*203T>A
NM_001290357.2:c.*261T>A NP_001277286.1:n.*261T>A
NR_110936.2:n.1084T>A