Canonical Allele Identifier: CA1558462347

Gene: DHFR

Linked Data

• dbSNP Id: rs1747952151
• gnomAD v4: 5-80628884-A-G

Genomic Alleles

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

Transcript Alleles

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