Canonical Allele Identifier: CA3586439
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 450672
dbSNP Id: rs771088509

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177604430T>C , CM000667.2:g.177604430T>C GRCh38
NC_000005.9:g.177031431T>C , CM000667.1:g.177031431T>C GRCh37
NC_000005.8:g.176964037T>C NCBI36
NG_015977.1:g.9313T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000029410.10:c.302T>C MANE Select ENSP00000029410.5:p.Phe101Ser
ENST00000029410.9:c.302T>C ENSP00000029410.5:p.Phe101Ser
ENST00000502420.1:n.281T>C
ENST00000505433.5:c.302T>C ENSP00000425591.1:p.Phe101Ser
ENST00000505468.1:c.-41T>C ENSP00000420886.1:n.-41T>C
ENST00000507061.1:c.119T>C ENSP00000423868.1:p.Phe40Ser
ENST00000510761.1:c.-41T>C ENSP00000423438.1:n.-41T>C
NM_007255.2:c.302T>C NP_009186.1:p.Phe101Ser
XM_005265805.2:c.-41T>C XP_005265862.1:n.-41T>C
XM_006714816.2:c.-198T>C XP_006714879.1:n.-198T>C
XM_011534421.1:c.-41T>C XP_011532723.1:n.-41T>C
XM_006714816.4:c.-198T>C XP_006714879.1:n.-198T>C
XM_017008999.2:c.-41T>C XP_016864488.1:n.-41T>C
NM_007255.3:c.302T>C MANE Select NP_009186.1:p.Phe101Ser