Canonical Allele Identifier: CA15843920
Gene: ITGA11 HGNC NCBI

Linked Data

dbSNP Id: rs16952059
gnomAD v2: 15-68718000-C-T
gnomAD v3: 15-68425661-C-T
gnomAD v4: 15-68425661-C-T
MyVariant Identifiers: chr15:g.68718000C>T (hg19) chr15:g.68425661C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68425661C>T , CM000677.2:g.68425661C>T GRCh38
NC_000015.9:g.68718000C>T , CM000677.1:g.68718000C>T GRCh37
NC_000015.8:g.66505054C>T NCBI36
NG_046911.1:g.11500G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315757.9:c.52+6354G>A MANE Select ENSP00000327290.7:n.52+6354G>A
ENST00000315757.8:c.52+6354G>A ENSP00000327290.7:n.52+6354G>A
ENST00000423218.6:c.52+6354G>A ENSP00000403392.2:n.52+6354G>A
NM_001004439.1:c.52+6354G>A NP_001004439.1:n.52+6354G>A
XM_011521363.1:c.52+6354G>A XP_011519665.1:n.52+6354G>A
XM_011521363.2:c.52+6354G>A XP_011519665.1:n.52+6354G>A
NM_001004439.2:c.52+6354G>A MANE Select NP_001004439.1:n.52+6354G>A
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