Canonical Allele Identifier: CA440618955
Gene:

Linked Data

gnomAD v4: 4-102500915-T-C
MyVariant Identifiers: chr4:g.103422072T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500915T>C , CM000666.2:g.102500915T>C GRCh38
NC_000004.11:g.103422072T>C , CM000666.1:g.103422072T>C GRCh37
NC_000004.10:g.103641104T>C NCBI36
NG_050628.1:g.4587T>C

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+334A>G XP_011530769.1:n.643+334A>G
NR_136202.1:n.48+1524A>G
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