Canonical Allele Identifier: CA11735861
Gene:

Linked Data

dbSNP Id: rs10519980
gnomAD v2: 4-149635025-C-T
gnomAD v3: 4-148713873-C-T
gnomAD v4: 4-148713873-C-T
MyVariant Identifiers: chr4:g.149635025C>T (hg19) chr4:g.148713873C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148713873C>T , CM000666.2:g.148713873C>T GRCh38
NC_000004.11:g.149635025C>T , CM000666.1:g.149635025C>T GRCh37
NC_000004.10:g.149854475C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741441.1:n.1746-152884C>T
Search 100 bp 5'
Search 100 bp 3'