Canonical Allele Identifier: CA362373565
Gene: B4GALT7 HGNC NCBI

Linked Data

dbSNP Id: rs1310598945

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177604399G>C , CM000667.2:g.177604399G>C GRCh38
NC_000005.9:g.177031400G>C , CM000667.1:g.177031400G>C GRCh37
NC_000005.8:g.176964006G>C NCBI36
NG_015977.1:g.9282G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000029410.10:c.271G>C MANE Select ENSP00000029410.5:p.Gly91Arg
ENST00000029410.9:c.271G>C ENSP00000029410.5:p.Gly91Arg
ENST00000502420.1:n.250G>C
ENST00000505433.5:c.271G>C ENSP00000425591.1:p.Gly91Arg
ENST00000505468.1:c.-72G>C ENSP00000420886.1:n.-72G>C
ENST00000507061.1:c.88G>C ENSP00000423868.1:p.Gly30Arg
ENST00000510761.1:c.-72G>C ENSP00000423438.1:n.-72G>C
NM_007255.2:c.271G>C NP_009186.1:p.Gly91Arg
XM_005265805.2:c.-72G>C XP_005265862.1:n.-72G>C
XM_006714816.2:c.-229G>C XP_006714879.1:n.-229G>C
XM_011534421.1:c.-72G>C XP_011532723.1:n.-72G>C
XM_006714816.4:c.-229G>C XP_006714879.1:n.-229G>C
XM_017008999.2:c.-72G>C XP_016864488.1:n.-72G>C
NM_007255.3:c.271G>C MANE Select NP_009186.1:p.Gly91Arg