Canonical Allele Identifier: CA14700600
Gene:

Linked Data

dbSNP Id: rs4141232
gnomAD v2: 19-29035556-T-C
gnomAD v3: 19-28544649-T-C
gnomAD v4: 19-28544649-T-C
MyVariant Identifiers: chr19:g.29035556T>C (hg19) chr19:g.28544649T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544649T>C , CM000681.2:g.28544649T>C GRCh38
NC_000019.9:g.29035556T>C , CM000681.1:g.29035556T>C GRCh37
NC_000019.8:g.33727396T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77869A>G
XR_243979.1:n.110-51626A>G
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