Canonical Allele Identifier: CA307005681
Gene:

Linked Data

dbSNP Id: rs191948367
gnomAD v3: 19-28544590-T-C
gnomAD v4: 19-28544590-T-C
MyVariant Identifiers: chr19:g.29035497T>C (hg19) chr19:g.28544590T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544590T>C , CM000681.2:g.28544590T>C GRCh38
NC_000019.9:g.29035497T>C , CM000681.1:g.29035497T>C GRCh37
NC_000019.8:g.33727337T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77810A>G
XR_243979.1:n.110-51567A>G
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