Canonical Allele Identifier: CA820839156
Gene:

Linked Data

dbSNP Id: rs1228746104
gnomAD v3: 6-151633532-T-C
gnomAD v4: 6-151633532-T-C
MyVariant Identifiers: chr6:g.151954667T>C (hg19) chr6:g.151633532T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633532T>C , CM000668.2:g.151633532T>C GRCh38
NC_000006.11:g.151954667T>C , CM000668.1:g.151954667T>C GRCh37
NC_000006.10:g.151996360T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3550T>C
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