Canonical Allele Identifier: CA2670965512

Gene: ALB

Linked Data

• gnomAD v4: 4-73414917-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414917T>C , CM000666.2:g.73414917T>C	GRCh38
NC_000004.11:g.74280634T>C , CM000666.1:g.74280634T>C	GRCh37
NC_000004.10:g.74499498T>C	NCBI36
NG_009291.1:g.15663T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1059-118T>C MANE Select	ENSP00000295897.4:n.1059-118T>C
ENST00000295897.8:c.1059-118T>C	ENSP00000295897.4:n.1059-118T>C
ENST00000401494.7:c.714-118T>C	ENSP00000384695.3:n.714-118T>C
ENST00000415165.6:c.483-118T>C	ENSP00000401820.2:n.483-118T>C
ENST00000476441.6:c.*338-118T>C	ENSP00000423727.1:n.*338-118T>C
ENST00000484992.1:n.379-118T>C
ENST00000503124.5:c.609-118T>C	ENSP00000421027.1:n.609-118T>C
ENST00000504043.1:n.62-118T>C
ENST00000505649.5:n.745-118T>C
ENST00000509063.5:c.1059-118T>C	ENSP00000422784.1:n.1059-118T>C
ENST00000511370.1:c.592-118T>C
ENST00000621085.4:c.491-189T>C	ENSP00000483421.1:n.491-189T>C
ENST00000621628.4:c.487-185T>C	ENSP00000480485.1:n.487-185T>C
NM_000477.5:c.1059-118T>C	NP_000468.1:n.1059-118T>C
NM_000477.6:c.1059-118T>C	NP_000468.1:n.1059-118T>C
NM_000477.7:c.1059-118T>C MANE Select	NP_000468.1:n.1059-118T>C