Canonical Allele Identifier: CA255899013
Gene:

Linked Data

dbSNP Id: rs1055403815
gnomAD v2: 13-105478649-A-G
gnomAD v3: 13-104826298-A-G
gnomAD v4: 13-104826298-A-G
MyVariant Identifiers: chr13:g.105478649A>G (hg19) chr13:g.104826298A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.104826298A>G , CM000675.2:g.104826298A>G GRCh38
NC_000013.10:g.105478649A>G , CM000675.1:g.105478649A>G GRCh37
NC_000013.9:g.104276650A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749993.1:n.242-2511T>C
XR_001749994.1:n.243+10905T>C
XR_001749995.1:n.253+10905T>C
XR_001749996.1:n.1897-2757A>G
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