Canonical Allele Identifier: CA7927694

Gene: XYLT1

Linked Data

• dbSNP Id: rs775309533
• ExAC: 16:17228300 T / C
• gnomAD v2: 16-17228300-T-C
• gnomAD v4: 16-17134443-T-C
• MyVariant Identifiers: chr16:g.17228300T>C (hg19) ; chr16:g.17134443T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134443T>C , CM000678.2:g.17134443T>C	GRCh38
NC_000016.9:g.17228300T>C , CM000678.1:g.17228300T>C	GRCh37
NC_000016.8:g.17135801T>C	NCBI36
NG_015843.1:g.341439A>G
NG_015843.2:g.341439A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.2027+30A>G MANE Select	ENSP00000261381.6:n.2027+30A>G
ENST00000261381.6:c.2027+30A>G	ENSP00000261381.6:n.2027+30A>G
NM_022166.3:c.2027+30A>G	NP_071449.1:n.2027+30A>G
XM_011522574.1:c.2027+30A>G	XP_011520876.1:n.2027+30A>G
XM_017023539.2:c.2027+30A>G	XP_016879028.1:n.2027+30A>G
XM_017023540.2:c.2027+30A>G	XP_016879029.1:n.2027+30A>G
NM_022166.4:c.2027+30A>G MANE Select	NP_071449.1:n.2027+30A>G