Canonical Allele Identifier: CA829017307
Gene:

Linked Data

dbSNP Id: rs1203936484
gnomAD v4: 6-8525281-C-T
MyVariant Identifiers: chr6:g.8525514C>T (hg19) chr6:g.8525281C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525281C>T , CM000668.2:g.8525281C>T GRCh38
NC_000006.11:g.8525514C>T , CM000668.1:g.8525514C>T GRCh37
NC_000006.10:g.8470513C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038979.1:n.626-33304C>T
NR_038980.1:n.649-33304C>T
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Search 100 bp 3'