Canonical Allele Identifier: CA145511532
Gene:

Linked Data

dbSNP Id: rs1027534078
gnomAD v2: 6-106253036-A-G
gnomAD v3: 6-105805161-A-G
gnomAD v4: 6-105805161-A-G
MyVariant Identifiers: chr6:g.106253036A>G (hg19) chr6:g.105805161A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805161A>G , CM000668.2:g.105805161A>G GRCh38
NC_000006.11:g.106253036A>G , CM000668.1:g.106253036A>G GRCh37
NC_000006.10:g.106359729A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24896T>C
XR_001744274.1:n.438+24896T>C
XR_001744275.1:n.337+24896T>C
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