Canonical Allele Identifier: CA806248918

Gene: ADAM19

Linked Data

• dbSNP Id: rs552122242
• gnomAD v3: 5-157543078-G-A
• gnomAD v4: 5-157543078-G-A
• MyVariant Identifiers: chr5:g.156970086G>A (hg19) ; chr5:g.157543078G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157543078G>A , CM000667.2:g.157543078G>A	GRCh38
NC_000005.9:g.156970086G>A , CM000667.1:g.156970086G>A	GRCh37
NC_000005.8:g.156902664G>A	NCBI36
NG_046960.1:g.37746C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.252-5087C>T MANE Select	ENSP00000257527.5:n.252-5087C>T
ENST00000257527.8:c.252-5087C>T	ENSP00000257527.4:n.252-5087C>T
ENST00000517905.1:c.252-5087C>T	ENSP00000428654.1:n.252-5087C>T
ENST00000517951.5:c.252-5087C>T	ENSP00000428376.1:n.252-5087C>T
NM_033274.4:c.252-5087C>T	NP_150377.1:n.252-5087C>T
XM_005266003.2:c.252-5087C>T	XP_005266060.1:n.252-5087C>T
NM_033274.5:c.252-5087C>T MANE Select	NP_150377.1:n.252-5087C>T