Canonical Allele Identifier: CA2674438752
Gene: DHFR HGNC NCBI

Linked Data

gnomAD v4: 5-80628874-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628874C>G , CM000667.2:g.80628874C>G GRCh38
NC_000005.9:g.79924693C>G , CM000667.1:g.79924693C>G GRCh37
NC_000005.8:g.79960449C>G NCBI36
NG_023304.1:g.31108G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.*213G>C MANE Select ENSP00000396308.2:n.*213G>C
ENST00000439211.6:c.*213G>C ENSP00000396308.2:n.*213G>C
ENST00000504396.1:c.*213G>C ENSP00000421334.1:n.*213G>C
ENST00000505337.5:c.*113G>C ENSP00000426474.1:n.*113G>C
ENST00000511032.5:c.*271G>C ENSP00000422732.1:n.*271G>C
ENST00000513048.5:n.658G>C
NM_000791.3:c.*213G>C NP_000782.1:n.*213G>C
NM_001290354.1:c.*213G>C NP_001277283.1:n.*213G>C
NM_001290357.1:c.*271G>C NP_001277286.1:n.*271G>C
NR_110936.1:n.1092G>C
NM_000791.4:c.*213G>C MANE Select NP_000782.1:n.*213G>C
NM_001290354.2:c.*213G>C NP_001277283.1:n.*213G>C
NM_001290357.2:c.*271G>C NP_001277286.1:n.*271G>C
NR_110936.2:n.1094G>C