Canonical Allele Identifier: CA255899019
Gene:

Linked Data

dbSNP Id: rs562219971
gnomAD v3: 13-104826316-G-A
gnomAD v4: 13-104826316-G-A
MyVariant Identifiers: chr13:g.105478667G>A (hg19) chr13:g.104826316G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.104826316G>A , CM000675.2:g.104826316G>A GRCh38
NC_000013.10:g.105478667G>A , CM000675.1:g.105478667G>A GRCh37
NC_000013.9:g.104276668G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749993.1:n.242-2529C>T
XR_001749994.1:n.243+10887C>T
XR_001749995.1:n.253+10887C>T
XR_001749996.1:n.1897-2739G>A
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