Canonical Allele Identifier: CA224399067

Gene: FOLR1

Linked Data

• dbSNP Id: rs1026111024
• MyVariant Identifiers: chr11:g.71901044C>T (hg19) ; chr11:g.72190000C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72190000C>T , CM000673.2:g.72190000C>T	GRCh38
NC_000011.9:g.71901044C>T , CM000673.1:g.71901044C>T	GRCh37
NC_000011.8:g.71578692C>T	NCBI36
NG_015863.1:g.5443C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.-9+241C>T	ENSP00000308137.4:n.-9+241C>T
ENST00000675784.1:c.-9+69C>T	ENSP00000502440.1:n.-9+69C>T
ENST00000312293.8:c.-9+241C>T	ENSP00000308137.4:n.-9+241C>T
ENST00000393681.6:c.-75+241C>T	ENSP00000377286.2:n.-75+241C>T
NM_000802.3:c.-9+69C>T	NP_000793.1:n.-9+69C>T
NM_016724.2:c.-75+241C>T	NP_057936.1:n.-75+241C>T
NM_016725.2:c.-9+241C>T	NP_057937.1:n.-9+241C>T
NM_016724.3:c.-75+241C>T	NP_057936.1:n.-75+241C>T
NM_016725.3:c.-9+241C>T	NP_057937.1:n.-9+241C>T