Canonical Allele Identifier: CA278645141
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs191322955
gnomAD v2: 16-17232854-G-A
gnomAD v3: 16-17138997-G-A
gnomAD v4: 16-17138997-G-A
MyVariant Identifiers: chr16:g.17232854G>A (hg19) chr16:g.17138997G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138997G>A , CM000678.2:g.17138997G>A GRCh38
NC_000016.9:g.17232854G>A , CM000678.1:g.17232854G>A GRCh37
NC_000016.8:g.17140355G>A NCBI36
NG_015843.1:g.336885C>T
NG_015843.2:g.336885C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-466C>T MANE Select ENSP00000261381.6:n.1588-466C>T
ENST00000261381.6:c.1588-466C>T ENSP00000261381.6:n.1588-466C>T
NM_022166.3:c.1588-466C>T NP_071449.1:n.1588-466C>T
XM_011522574.1:c.1588-466C>T XP_011520876.1:n.1588-466C>T
XM_017023539.2:c.1588-466C>T XP_016879028.1:n.1588-466C>T
XM_017023540.2:c.1588-466C>T XP_016879029.1:n.1588-466C>T
NM_022166.4:c.1588-466C>T MANE Select NP_071449.1:n.1588-466C>T
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