Canonical Allele Identifier: CA362376866

Gene: B4GALT7

Linked Data

• MyVariant Identifiers: chr5:g.177035962C>T (hg19) ; chr5:g.177608961C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608961C>T , CM000667.2:g.177608961C>T	GRCh38
NC_000005.9:g.177035962C>T , CM000667.1:g.177035962C>T	GRCh37
NC_000005.8:g.176968568C>T	NCBI36
NG_015977.1:g.13844C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.775C>T MANE Select	ENSP00000029410.5:p.His259Tyr
ENST00000029410.9:c.775C>T	ENSP00000029410.5:p.His259Tyr
ENST00000505145.1:n.1873C>T
ENST00000505433.5:c.*281C>T	ENSP00000425591.1:n.*281C>T
ENST00000515353.1:n.1597C>T
NM_007255.2:c.775C>T	NP_009186.1:p.His259Tyr
XM_005265805.2:c.433C>T	XP_005265862.1:p.His145Tyr
XM_006714816.2:c.295C>T	XP_006714879.1:p.His99Tyr
XM_011534421.1:c.433C>T	XP_011532723.1:p.His145Tyr
XM_006714816.4:c.295C>T	XP_006714879.1:p.His99Tyr
XM_017008999.2:c.433C>T	XP_016864488.1:p.His145Tyr
NM_007255.3:c.775C>T MANE Select	NP_009186.1:p.His259Tyr