Canonical Allele Identifier: CA15674567
Gene: SFR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10883969

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104124358C>T , CM000672.2:g.104124358C>T GRCh38
NC_000010.10:g.105884116C>T , CM000672.1:g.105884116C>T GRCh37
NC_000010.9:g.105874106C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001002759.1:c.546+234C>T VV NP_001002759.1:p.=
NM_145247.4:c.507+234C>T VV NP_660290.3:p.=
XM_005269521.2:c.732+234C>T XP_005269578.1:p.=
XM_005269521.3:c.732+234C>T XP_005269578.1:p.=
XM_017015672.1:c.507+234C>T XP_016871161.1:p.=
ENST00000369727.3:c.546+234C>T ENSP00000358742.3:p.=
ENST00000369729.7:c.507+234C>T ENSP00000358744.3:p.=