Canonical Allele Identifier: CA278672613
Gene:

Linked Data

dbSNP Id: rs977640257
MyVariant Identifiers: chr16:g.16237759G>A (hg19) chr16:g.16143902G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16143902G>A , CM000678.2:g.16143902G>A GRCh38
NC_000016.9:g.16237759G>A , CM000678.1:g.16237759G>A GRCh37
NC_000016.8:g.16145260G>A NCBI36
NG_028268.1:g.199326G>A
NG_028268.2:g.199326G>A

Transcript Alleles

HGVS Amino-acid change
XR_933134.1:n.150G>A
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