Canonical Allele Identifier: CA569468977
Gene:

Linked Data

dbSNP Id: rs1483608525
gnomAD v2: 6-106253017-T-C
gnomAD v3: 6-105805142-T-C
gnomAD v4: 6-105805142-T-C
MyVariant Identifiers: chr6:g.106253017T>C (hg19) chr6:g.105805142T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805142T>C , CM000668.2:g.105805142T>C GRCh38
NC_000006.11:g.106253017T>C , CM000668.1:g.106253017T>C GRCh37
NC_000006.10:g.106359710T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24915A>G
XR_001744274.1:n.438+24915A>G
XR_001744275.1:n.337+24915A>G
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