Canonical Allele Identifier: CA362372396
Gene: B4GALT7 HGNC NCBI

Linked Data

dbSNP Id: rs1257503347

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177604193C>T , CM000667.2:g.177604193C>T GRCh38
NC_000005.9:g.177031194C>T , CM000667.1:g.177031194C>T GRCh37
NC_000005.8:g.176963800C>T NCBI36
NG_015977.1:g.9076C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000029410.10:c.65C>T MANE Select ENSP00000029410.5:p.Ser22Phe
ENST00000029410.9:c.65C>T ENSP00000029410.5:p.Ser22Phe
ENST00000502420.1:n.130-86C>T
ENST00000505433.5:c.65C>T ENSP00000425591.1:p.Ser22Phe
ENST00000505468.1:c.-278C>T ENSP00000420886.1:n.-278C>T
ENST00000510761.1:c.-278C>T ENSP00000423438.1:n.-278C>T
NM_007255.2:c.65C>T NP_009186.1:p.Ser22Phe
XM_005265805.2:c.-278C>T XP_005265862.1:n.-278C>T
XM_006714816.2:c.-435C>T XP_006714879.1:n.-435C>T
XM_011534421.1:c.-278C>T XP_011532723.1:n.-278C>T
XM_006714816.4:c.-435C>T XP_006714879.1:n.-435C>T
XM_017008999.2:c.-278C>T XP_016864488.1:n.-278C>T
NM_007255.3:c.65C>T MANE Select NP_009186.1:p.Ser22Phe