Canonical Allele Identifier: CA440620351
Gene:

Linked Data

dbSNP Id: rs1446700620
gnomAD v3: 4-102501218-G-A
gnomAD v4: 4-102501218-G-A
MyVariant Identifiers: chr4:g.103422375G>A (hg19) chr4:g.102501218G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501218G>A , CM000666.2:g.102501218G>A GRCh38
NC_000004.11:g.103422375G>A , CM000666.1:g.103422375G>A GRCh37
NC_000004.10:g.103641407G>A NCBI36
NG_050628.1:g.4890G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+31C>T XP_011530769.1:n.643+31C>T
NR_136202.1:n.48+1221C>T
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