Canonical Allele Identifier: CA553826991
Gene:

Linked Data

dbSNP Id: rs10005603
gnomAD v2: 4-105844273-T-C
gnomAD v3: 4-104923116-T-C
gnomAD v4: 4-104923116-T-C
MyVariant Identifiers: chr4:g.105844273T>C (hg19) chr4:g.104923116T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.104923116T>C , CM000666.2:g.104923116T>C GRCh38
NC_000004.11:g.105844273T>C , CM000666.1:g.105844273T>C GRCh37
NC_000004.10:g.106063722T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939034.1:n.79-495T>C
XR_939035.1:n.79-495T>C
Search 100 bp 5'
Search 100 bp 3'