Canonical Allele Identifier: CA13796861
Gene:

Linked Data

dbSNP Id: rs2209852
gnomAD v2: 13-95517622-A-G
gnomAD v3: 13-94865368-A-G
gnomAD v4: 13-94865368-A-G
MyVariant Identifiers: chr13:g.95517622A>G (hg19) chr13:g.94865368A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94865368A>G , CM000675.2:g.94865368A>G GRCh38
NC_000013.10:g.95517622A>G , CM000675.1:g.95517622A>G GRCh37
NC_000013.9:g.94315623A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110754.1:n.257-40096A>G
Search 100 bp 5'
Search 100 bp 3'