Canonical Allele Identifier: CA2674438766
Gene: DHFR HGNC NCBI

Linked Data

gnomAD v4: 5-80628887-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628887T>C , CM000667.2:g.80628887T>C GRCh38
NC_000005.9:g.79924706T>C , CM000667.1:g.79924706T>C GRCh37
NC_000005.8:g.79960462T>C NCBI36
NG_023304.1:g.31095A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.*200A>G MANE Select ENSP00000396308.2:n.*200A>G
ENST00000439211.6:c.*200A>G ENSP00000396308.2:n.*200A>G
ENST00000504396.1:c.*200A>G ENSP00000421334.1:n.*200A>G
ENST00000505337.5:c.*100A>G ENSP00000426474.1:n.*100A>G
ENST00000511032.5:c.*258A>G ENSP00000422732.1:n.*258A>G
ENST00000513048.5:n.645A>G
NM_000791.3:c.*200A>G NP_000782.1:n.*200A>G
NM_001290354.1:c.*200A>G NP_001277283.1:n.*200A>G
NM_001290357.1:c.*258A>G NP_001277286.1:n.*258A>G
NR_110936.1:n.1079A>G
NM_000791.4:c.*200A>G MANE Select NP_000782.1:n.*200A>G
NM_001290354.2:c.*200A>G NP_001277283.1:n.*200A>G
NM_001290357.2:c.*258A>G NP_001277286.1:n.*258A>G
NR_110936.2:n.1081A>G