Canonical Allele Identifier: CA278644968
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs905002646
gnomAD v2: 16-17232674-T-G
gnomAD v3: 16-17138817-T-G
gnomAD v4: 16-17138817-T-G
MyVariant Identifiers: chr16:g.17232674T>G (hg19) chr16:g.17138817T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138817T>G , CM000678.2:g.17138817T>G GRCh38
NC_000016.9:g.17232674T>G , CM000678.1:g.17232674T>G GRCh37
NC_000016.8:g.17140175T>G NCBI36
NG_015843.1:g.337065A>C
NG_015843.2:g.337065A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-286A>C MANE Select ENSP00000261381.6:n.1588-286A>C
ENST00000261381.6:c.1588-286A>C ENSP00000261381.6:n.1588-286A>C
NM_022166.3:c.1588-286A>C NP_071449.1:n.1588-286A>C
XM_011522574.1:c.1588-286A>C XP_011520876.1:n.1588-286A>C
XM_017023539.2:c.1588-286A>C XP_016879028.1:n.1588-286A>C
XM_017023540.2:c.1588-286A>C XP_016879029.1:n.1588-286A>C
NM_022166.4:c.1588-286A>C MANE Select NP_071449.1:n.1588-286A>C
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