Canonical Allele Identifier: CA814449637

Gene: DHFR

Linked Data

• dbSNP Id: rs1290049984
• MyVariant Identifiers: chr5:g.79924812A>G (hg19) ; chr5:g.80628993A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628993A>G , CM000667.2:g.80628993A>G	GRCh38
NC_000005.9:g.79924812A>G , CM000667.1:g.79924812A>G	GRCh37
NC_000005.8:g.79960568A>G	NCBI36
NG_023304.1:g.30989T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*94T>C MANE Select	ENSP00000396308.2:n.*94T>C
ENST00000439211.6:c.*94T>C	ENSP00000396308.2:n.*94T>C
ENST00000504396.1:c.*94T>C	ENSP00000421334.1:n.*94T>C
ENST00000505337.5:c.*48+46T>C	ENSP00000426474.1:n.*48+46T>C
ENST00000511032.5:c.*152T>C	ENSP00000422732.1:n.*152T>C
ENST00000513048.5:n.539T>C
NM_000791.3:c.*94T>C	NP_000782.1:n.*94T>C
NM_001290354.1:c.*94T>C	NP_001277283.1:n.*94T>C
NM_001290357.1:c.*152T>C	NP_001277286.1:n.*152T>C
NR_110936.1:n.973T>C
NM_000791.4:c.*94T>C MANE Select	NP_000782.1:n.*94T>C
NM_001290354.2:c.*94T>C	NP_001277283.1:n.*94T>C
NM_001290357.2:c.*152T>C	NP_001277286.1:n.*152T>C
NR_110936.2:n.975T>C