Canonical Allele Identifier: CA497677271

Linked Data

gnomAD v4: 17-4932725-C-T
MyVariant Identifiers: chr17:g.4836020C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4932725C>T , CM000679.2:g.4932725C>T GRCh38
NC_000017.10:g.4836020C>T , CM000679.1:g.4836020C>T GRCh37
NC_000017.9:g.4776800C>T NCBI36
NG_008767.2:g.5431C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000329125.6:c.121C>T (GP1BA) MANE Select ENSP00000329380.5:p.Leu41=
ENST00000649830.1:c.-888+1617G>A (CHRNE) ENSP00000496907.1:n.-888+1617G>A
ENST00000329125.5:c.121C>T (GP1BA) ENSP00000329380.5:p.Leu41=
ENST00000611961.1:c.121C>T (GP1BA) ENSP00000484439.1:p.Leu41=
NM_000173.6:c.121C>T (GP1BA) NP_000164.5:p.Leu41=
NM_000173.7:c.121C>T (GP1BA) MANE Select NP_000164.5:p.Leu41=