Canonical Allele Identifier: CA11934763
Gene: DHFR HGNC NCBI

Linked Data

dbSNP Id: rs1643649

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80643630T>C , CM000667.2:g.80643630T>C GRCh38
NC_000005.9:g.79939449T>C , CM000667.1:g.79939449T>C GRCh37
NC_000005.8:g.79975205T>C NCBI36
NG_023304.1:g.16352A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000439211.7:c.243-5621A>G MANE Select ENSP00000396308.2:p.=
ENST00000439211.6:c.243-5621A>G ENSP00000396308.2:p.=
ENST00000504396.1:c.87-5621A>G ENSP00000421334.1:p.=
ENST00000505337.5:c.243-5621A>G ENSP00000426474.1:p.=
ENST00000508282.1:n.201-5621A>G
ENST00000511032.5:c.243-5621A>G ENSP00000422732.1:p.=
ENST00000513048.5:n.250+5759A>G
NM_000791.3:c.243-5621A>G NP_000782.1:p.=
NM_001290354.1:c.87-5621A>G NP_001277283.1:p.=
NM_001290357.1:c.243-5621A>G NP_001277286.1:p.=
NR_110936.1:n.684+5759A>G
NM_000791.4:c.243-5621A>G MANE Select NP_000782.1:p.=
NM_001290354.2:c.87-5621A>G NP_001277283.1:p.=
NM_001290357.2:c.243-5621A>G NP_001277286.1:p.=
NR_110936.2:n.686+5759A>G