Canonical Allele Identifier: CA12281667
Gene:

Linked Data

dbSNP Id: rs1853665
gnomAD v2: 6-150298842-C-T
gnomAD v3: 6-149977706-C-T
gnomAD v4: 6-149977706-C-T
MyVariant Identifiers: chr6:g.150298842C>T (hg19) chr6:g.149977706C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149977706C>T , CM000668.2:g.149977706C>T GRCh38
NC_000006.11:g.150298842C>T , CM000668.1:g.150298842C>T GRCh37
NC_000006.10:g.150340535C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406262.1:n.236C>T
Search 100 bp 5'
Search 100 bp 3'