Canonical Allele Identifier: CA230606054
Gene:

Linked Data

dbSNP Id: rs757519745
gnomAD v2: 11-128740868-G-A
gnomAD v3: 11-128870973-G-A
gnomAD v4: 11-128870973-G-A
MyVariant Identifiers: chr11:g.128740868G>A (hg19) chr11:g.128870973G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128870973G>A , CM000673.2:g.128870973G>A GRCh38
NC_000011.9:g.128740868G>A , CM000673.1:g.128740868G>A GRCh37
NC_000011.8:g.128246078G>A NCBI36
NG_009379.1:g.1401C>T

Transcript Alleles

HGVS Amino-acid Change
XR_948172.1:n.5938C>T
XR_948173.1:n.5627C>T
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Search 100 bp 3'