Canonical Allele Identifier: CA772085998

Gene: HCRT

Linked Data

• dbSNP Id: rs1475916460
• gnomAD v3: 17-42184702-G-T
• gnomAD v4: 17-42184702-G-T
• MyVariant Identifiers: chr17:g.40336720G>T (hg19) ; chr17:g.42184702G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42184702G>T , CM000679.2:g.42184702G>T	GRCh38
NC_000017.10:g.40336720G>T , CM000679.1:g.40336720G>T	GRCh37
NC_000017.9:g.37590246G>T	NCBI36
NG_011448.1:g.5751C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293330.1:c.22-174C>A MANE Select	ENSP00000293330.1:n.22-174C>A
NM_001524.1:c.22-174C>A MANE Select	NP_001515.1:n.22-174C>A