Canonical Allele Identifier: CA2738959064

Gene: FRMD7

Linked Data

• dbSNP Id: rs1929196577

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.132127939C>A , CM000685.2:g.132127939C>A	GRCh38
NC_000023.10:g.131261967C>A , CM000685.1:g.131261967C>A	GRCh37
NC_000023.9:g.131089648C>A	NCBI36
NG_012347.1:g.5084G>T , LRG_867:g.5084G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298542.9:c.-95G>T MANE Select	ENSP00000298542.3:n.-95G>T
ENST00000298542.8:c.-95G>T	ENSP00000298542.3:n.-95G>T
NM_001306193.1:c.-95G>T	NP_001293122.1:n.-95G>T
NM_194277.2:c.-95G>T , LRG_867t1:c.-95G>T	NP_919253.1:n.-95G>T
NM_001306193.2:c.-95G>T	NP_001293122.1:n.-95G>T
NM_194277.3:c.-95G>T MANE Select	NP_919253.1:n.-95G>T